Integra LifeSciences Holdings Corporation (NASDAQ: IART), a
leading global medical technology company, today reported financial
results for the third quarter ending September 30, 2024.
Third Quarter 2024 Highlights
- Third quarter revenues of $380.8 million decreased 0.4% on a
reported basis and 8.6% on an organic basis compared to the prior
year. Revenue decreased 10.3% on an organic basis excluding
Boston.
- Third quarter GAAP earnings per diluted share of $(0.14),
compared to $0.24 in the prior year; adjusted earnings per diluted
share of $0.41, compared to $0.76 in the prior year.
- Shipping holds communicated during the second quarter earnings
call are releasing in line with expectations.
- Integra Skin production is on pace to meet historical revenue
run rates for the fourth quarter.
- Updating full-year 2024 revenue guidance to a range of $1.609
billion to $1.619 billion and adjusted EPS guidance to a range of
$2.41 to $2.49 per share.
- The Company announced Mojdeh Poul as Integra’s next president
and chief executive officer.
“Our third-quarter results highlight the early progress we are
making to identify and remediate the gaps in our quality management
system," said Jan De Witte, president and CEO of Integra
LifeSciences. "We are progressing with the implementation of our
compliance master plan across our manufacturing and supply chain
operations, which will position us to meet robust market demand and
more consistently and reliably deliver to customers, patients, and
shareholders."
Third Quarter 2024 Consolidated Performance
Total reported revenues of $380.8 million decreased 0.4% on a
reported basis and 8.6% on an organic basis compared to the prior
year. Revenue decreased 10.3% on an organic basis excluding
Boston.
The Company reported GAAP gross margin of 52.6%, compared to
57.1% in the third quarter of 2023. Adjusted gross margin was
63.0%, compared to 64.6% in the prior year.
Adjusted EBITDA for the third quarter of 2024 was $61.8 million,
or 16.2% of revenue, compared to $88.1 million, or 23.0% of
revenue, in the prior year.
The Company reported a GAAP net loss of $(10.7) million, or
$(0.14) per diluted share, in the third quarter of 2024, compared
to GAAP net income of $19.5 million, or $0.24 per diluted share, in
the prior year.
Adjusted net income for the third quarter of 2024 was $31.7
million, or $0.41 per diluted share, compared to $60.5 million, or
$0.76 per diluted share, in the prior year.
Third Quarter 2024 Segment Performance
Codman Specialty Surgical
(~70% of Revenues)
Total revenues were $270.8 million, representing reported growth
of 1.0% and an organic decline of 10.7% compared to the third
quarter of 2023.
- Sales in Neurosurgery declined 16.0% on an organic basis
- The decline was driven primarily by temporary shipping holds in
CSF management and Neuro monitoring, which have largely been
resolved within the third quarter, as well as supply challenges in
Dural access and repair
- Advanced energy grew mid-single digits driven by CUSA® capital
and CUSA disposables
- Sales in Instruments grew 8.7% on an organic basis
- ENT reported revenue grew substantially due to the Acclarent
acquisition
Tissue Technologies (~30%
of Revenues)
Total revenues were $110.1 million, representing a reported
decline of 3.6% and organic decline of 3.7% compared to the third
quarter of 2023. Tissue Technologies sales were down 9.4% excluding
sales of the Company’s products manufactured in Boston. Key drivers
for the quarter include:
- Low double-digit decline in Integra Skin due to production
challenges
- Low double-digit growth in DuraSorb®, MicroMatrix® and
Cytal®
- Sales in private label grew 13.3% on an organic basis
CEO Transition Update
Today, the Company announced Mojdeh Poul as Integra’s next
president and chief executive officer. Ms. Poul succeeds Jan De
Witte, who previously announced he will retire as president and
chief executive officer. Ms. Poul will join Integra on January 6,
2025, at which time she will also be appointed to Integra’s board
of directors.
Advancing our Strategy
- Continued strong demand for Integra's diverse portfolio of
leading brands
- Advancing the compliance master plan and investments in supply
reliability
- Neurosurgery shipping holds clearing in line with
expectations
- Integra Skin production is on pace to meet historical revenue
run rates for the fourth quarter
- Began installing equipment in Braintree facility
- Continued integration success with the Acclarent ENT
products
- Growth in DuraSorb® and UBM portfolio remains strong
Balance Sheet, Cash Flow and Capital
Allocation
The Company generated cash flow from operations of $22.5 million
in the quarter. Total balance sheet debt and net debt at the end of
the quarter were $1.81 billion and $1.54 billion, respectively, and
the consolidated total leverage ratio was 4.0x.
As of quarter end, the Company had total liquidity of
approximately $1.18 billion, including $277 million in cash plus
short-term investments and the remainder available under its
revolving credit facility.
2024 Outlook
For the fourth quarter 2024, the Company expects reported
revenues in the range of $441 million to $451 million, representing
reported growth of 11.1% to 13.6% and organic growth of 2.0% to
4.5%. Fourth quarter guidance reflects the integration of
Acclarent, stepped up revenue from progress clearing the
third-quarter shipping holds, improved production for Integra Skin,
partially offset by additional quality holds. The Company expects
adjusted EPS in a range of $0.81 to $0.89.
For the full year 2024, the Company is updating its revenue and
adjusted EPS ranges of $1.609 billion to $1.619 billion and $2.41
to $2.49, respectively. The revenue range represents reported
growth of 4.4% to 5.0% and organic growth of -1.7% to -1.0%.
The Company’s organic sales growth guidance for the fourth
quarter and the full year excludes acquisitions and divestitures,
as well as the effects of foreign currency.
Conference Call and Presentation Available
Online
Integra has scheduled a conference call for 8:30 a.m. ET on
Monday November 4, 2024, to discuss third quarter 2024 financial
results and forward-looking financial guidance. The conference call
will be hosted by Integra's senior management team and will be open
to all listeners. Additional forward-looking information may be
discussed in a question-and-answer session following the call.
Integra's management team will reference a presentation during the
conference call, which can be found on the Investor section of the
website at investor.integralife.com.
A live webcast will be available on the Investors section of the
Company’s website at investor.integralife.com. For those planning
to participate on the call, register here to receive dial-in
details and an individual pin. While not required, it is
recommended to join 10 minutes prior to the event’s start. A
webcast replay of the conference call will be available on the
Investors section of the Company’s website following the call.
About Integra
At Integra LifeSciences, we are driven by our purpose of
restoring patients’ lives. We innovate treatment pathways to
advance patient outcomes and set new standards of surgical,
neurologic, and regenerative care. We offer a comprehensive
portfolio of high quality, leadership brands. For the latest news
and information about Integra and its products, please visit
www.integralife.com.
Forward-Looking Statements
This news release contains forward-looking statements within the
meaning of the Private Securities Litigation Reform Act of 1995
that involve risks and uncertainties and reflect the Company's
judgment as of the date of this release. All statements, other than
statements of historical fact, are statements that could be deemed
forward-looking statements. Some of these forward-looking
statements may contain words like “will,” “believe,” “may,”
“could,” “would,” “might,” “possible,” “should,” “expect,”
“intend,” "forecast," "guidance," “plan,” “anticipate,” "target,"
or “continue,” the negative of these words, other terms of similar
meaning or they may use future dates. Forward-looking statements
contained in this news release include, but are not limited to,
statements concerning: future financial performance, including
projections for revenues, expected revenue growth (both reported
and organic), GAAP and adjusted net income, GAAP and adjusted
earnings per diluted share, non-GAAP adjustments such as
divestiture, acquisition and integration-related charges,
intangible asset amortization, structural optimization charges, EU
Medical Device Regulation-related charges, charges related to the
voluntary global recall of all products manufactured at the
Company’s facility in Boston, Massachusetts and the transition of
Boston-related manufacturing operations to the Company’s Braintree,
Massachusetts facility, and income tax expense (benefit) related to
non-GAAP adjustments and other items; and the Company’s
expectations and plans with respect to business and operational
performance, strategic initiatives, capabilities, resources,
product development, product availability and regulatory approvals,
including expectations regarding the implementation and efficacy of
a compliance master plan to improve the Company's quality system.
It is important to note that the Company’s goals and expectations
are not predictions of actual performance. Such forward-looking
statements involve risks and uncertainties that could cause actual
results to differ materially from predicted or expected results.
Such risks and uncertainties include, but are not limited, to the
following: the ongoing and possible future effects of global
challenges, including macroeconomic uncertainties, inflation,
supply chain disruptions, trade regulation and tariffs, bank
failures and other economic disruptions, and U.S. and global
recession concerns, on the Company’s customers and on the Company’s
business, financial condition, results of operations and cash
flows; the Company's ability to execute its operating plan
effectively; the Company’s ability to successfully integrate
Acclarent and other acquired businesses; the Company’s ability to
achieve sales growth in a timely fashion; the Company's ability to
manufacture and ship sufficient quantities of its products to meet
its customers' demands; the ability of third-party suppliers to
supply us with raw materials and finished products; global
macroeconomic and political conditions, including the war in
Ukraine and the conflict in Israel and Gaza; the Company's ability
to manage its direct sales channels effectively; the sales
performance of third-party distributors on whom the Company relies
to generate revenue for certain products and geographic regions;
the Company's ability to access and maintain relationships with
customers of acquired entities and businesses; physicians'
willingness to adopt and third-party payors' willingness to provide
or maintain reimbursement for the Company's recently launched,
planned and existing products; initiatives launched by the
Company's competitors; downward pricing pressures from customers;
the Company's ability to secure regulatory approval for products in
development; the Company's ability to remediate quality systems
violations; difficulties in implementing the Company’s compliance
master plan and realizing the benefits contemplated thereby within
the anticipated timeframe, or at all; difficulties or delays in
obtaining and maintaining required regulatory approvals related to
the transition of the manufacturing to the Company’s Braintree
manufacturing facility; the possibility that costs or difficulties
related to building and the operationalization of the Braintree
facility or the transition of manufacturing activities from the
Company’s Boston facility to the Braintree facility will be greater
than expected; fluctuations in hospitals' spending for capital
equipment; uncertainties inherent in the development of new
products and the enhancement of existing products, including FDA
approval and/or clearance and other regulatory risks, technical
risks, cost overruns and delays; the Company's ability to comply
with regulations regarding products of human origin and products
containing materials derived from animal source; difficulties in
controlling expenses, including costs to procure and manufacture
the Company’s products; the ability of the Company to successfully
manage leadership and organizational changes and the impact of
changes in management or staff levels; the impact of goodwill and
intangible asset impairment charges if future operating results of
acquired businesses are significantly less than the results
anticipated at the time of the acquisitions, the Company's ability
to leverage its existing selling organizations and administrative
infrastructure; the Company's ability to increase product sales and
gross margins, and control non-product costs; the Company’s ability
to achieve anticipated growth rates, margins and scale and execute
its strategy generally; the amount and timing of divestiture,
acquisition and integration-related costs; the geographic
distribution of where the Company generates its taxable income; new
U.S. and foreign government laws and regulations, and changes in
existing laws, regulations and enforcement guidance, which affect
areas of our operations including, but not limited to, those
affecting the health care industry, including the EU Medical Device
Regulation; the scope, duration and effect of U.S. and
international governmental, regulatory, fiscal, monetary and public
health responses to any future public health crises; fluctuations
in foreign currency exchange rates; the amount of our bank
borrowings outstanding and other factors influencing liquidity;
potential negative impacts resulting from environmental, social and
governance matters; and the economic, competitive, governmental,
technological, and other risk factors and uncertainties identified
under the heading “Risk Factors” included in Item 1A of Integra's
Annual Report on Form 10-K for the year ended December 31, 2023 and
information contained in subsequent filings with the Securities and
Exchange Commission.
These forward-looking statements are made only as of the date
hereof, and the Company undertakes no obligation to update or
revise the forward-looking statements, whether as a result of new
information, future events, or otherwise, except as otherwise
required by law.
Discussion of Adjusted Financial Measures
In addition to our GAAP results, we provide certain non-GAAP
measures, including organic revenues, organic revenues excluding
Boston, adjusted earnings before interest, taxes, depreciation and
amortization (“EBITDA”), adjusted net income, adjusted gross
profit, adjusted gross margin, adjusted earnings per diluted share,
free cash flow, adjusted free cash flow conversion, and net debt.
Organic revenues consist of total revenues excluding the effects of
currency exchange rates, revenues from current-period acquisitions
and product divestitures. Organic revenues excluding Boston consist
of total revenues, excluding (i) the effects of currency exchange
rates, revenues from current-period acquisitions and product
divestitures and (ii) revenues associated with Boston produced
products including sales reported prior to the manufacturing
stoppage and voluntary global recall of all products manufactured
at the Company’s Boston, Massachusetts facility and distributed
between March 1, 2018 and May 22, 2023, as previously disclosed in
the Company’s Current Report on Form 8-K filed with the Securities
and Exchange Commission on May 23, 2023 (the “recall”), and the
impact of sales return provisions recorded. Adjusted EBITDA
consists of GAAP net income excluding: (i) depreciation and
amortization; (ii) other income (expense); (iii) interest income
and expense; (iv) income tax expense (benefit); and (v) those
operating expenses also excluded from adjusted net income. The
measure of adjusted net income consists of GAAP net income,
excluding: (i) structural optimization charges; (ii) divestiture,
acquisition and integration-related charges; (iii) EU Medical
Device Regulation-related charges; (iv) charges related to the
recall and the transition of Boston-related manufacturing
operations to the Company’s Braintree, Massachusetts facility; (v)
intangible asset amortization expense; and (vi) income tax impact
from adjustments. The measure of adjusted gross margin is
calculated by dividing adjusted gross profit by total revenues.
Adjusted gross profit consists of GAAP gross profit adjusted for:
(i) structural optimization charges; (ii) divestiture, acquisition
and integration-related charges; (iii) charges related to the
recall and the transition of Boston-related manufacturing
operations to the Company’s Braintree, Massachusetts facility; (iv)
EU Medical Device Regulation-related charges; and (v) intangible
asset amortization expense. The adjusted earnings per diluted share
measure is calculated by dividing adjusted net income attributable
to diluted shares by diluted weighted average shares outstanding.
The measure of free cash flow consists of GAAP net cash provided by
operating activities less purchases of property and equipment. The
adjusted free cash flow conversion measure is calculated by
dividing free cash flow by adjusted net income. The measure of net
debt consists of GAAP total debt (excluding deferred financing
costs) less short-term investments, cash and cash equivalents.
Reconciliations of GAAP revenues to organic revenues, GAAP
revenues to organic revenues excluding Boston, GAAP net income to
adjusted EBITDA, and adjusted net income, GAAP gross profit to
adjusted gross profit, GAAP gross margin to adjusted gross margin,
GAAP total debt to net debt, and GAAP earnings per diluted share to
adjusted earnings per diluted share all for the quarter ended
September 30, 2024 and 2023, and the GAAP operating cash flow to
free cash flow and adjusted free cash flow conversion for the
quarters ended September 30, 2024 and 2023, appear in the financial
tables in this release.
The Company believes that the presentation of organic revenues
and the other non-GAAP measures provide important supplemental
information to management and investors regarding financial and
business trends relating to the Company's financial condition and
results of operations. For further information regarding why
Integra believes that these non-GAAP financial measures provide
useful information to investors, the specific manner in which
management uses these measures, and some of the limitations
associated with the use of these measures, please refer to the
Company's Current Report on Form 8-K regarding this earnings press
release filed today with the Securities and Exchange Commission.
This Current Report on Form 8-K is available on the SEC's website
at www.sec.gov or on our website at
http://www.integralife.com.
Investor Relations
Contact:
Chris Ward(609) 772-7736chris.ward@integralife.com
Media Contact:
Laurene Isip(609) 208-8121laurene.isip@integralife.com
|
INTEGRA LIFESCIENCES HOLDINGS CORPORATIONCONDENSED CONSOLIDATED
STATEMENTS OF OPERATIONS(UNAUDITED) |
(In thousands, except per share amounts) |
|
|
Three Months Ended September 30, |
|
|
2024 |
|
|
|
2023 |
|
Total revenues, net |
$ |
380,834 |
|
|
$ |
382,421 |
|
|
|
|
|
Costs and expenses: |
|
|
|
Cost of goods sold |
|
180,596 |
|
|
|
164,076 |
|
Research and development |
|
27,435 |
|
|
|
26,596 |
|
Selling, general and
administrative |
|
177,193 |
|
|
|
161,948 |
|
Intangible asset
amortization |
|
3,760 |
|
|
|
3,208 |
|
Total costs and expenses |
|
388,984 |
|
|
|
355,828 |
|
|
|
|
|
Operating income (loss) |
|
(8,150 |
) |
|
|
26,593 |
|
|
|
|
|
Interest income |
|
5,049 |
|
|
|
4,607 |
|
Interest expense |
|
(19,373 |
) |
|
|
(13,062 |
) |
Other income, net |
|
2,112 |
|
|
|
471 |
|
Income before income
taxes |
|
(20,362 |
) |
|
|
18,609 |
|
Income tax expense
(benefit) |
|
(9,667 |
) |
|
|
(888 |
) |
Net income (loss) |
|
(10,695 |
) |
|
$ |
19,497 |
|
|
|
|
|
Net income per share: |
|
|
|
Diluted net income (loss) per
share |
$ |
(0.14 |
) |
|
$ |
0.24 |
|
|
|
|
|
Weighted average common shares
outstanding for diluted net income per share |
|
76,448 |
|
|
|
79,811 |
|
|
The following table presents revenues disaggregated by the major
sources for the three months ended September 30, 2024 and 2023
(amounts in thousands):
|
|
Three Months Ended September 30, |
|
|
2024 |
|
|
2023 |
|
Change |
Neurosurgery |
$ |
175,956 |
|
|
209,229 |
|
(15.9 |
)% |
Instruments(2) |
|
54,238 |
|
|
49,920 |
|
8.6 |
% |
ENT(2) |
|
40,588 |
|
|
9,056 |
|
348.2 |
% |
Total Codman Specialty
Surgical |
|
270,782 |
|
|
268,205 |
|
1.0 |
% |
|
|
|
|
Wound Reconstruction and
Care |
|
80,461 |
|
|
88,071 |
|
(8.6 |
)% |
Private Label |
|
29,592 |
|
|
26,145 |
|
13.2 |
% |
Total Tissue Technologies |
|
110,053 |
|
|
114,216 |
|
(3.6 |
)% |
Total reported revenues |
$ |
380,835 |
|
$ |
382,421 |
|
(0.4 |
)% |
|
|
|
|
Impact of changes in currency
exchange rates |
|
(185 |
) |
|
— |
|
|
Less contribution of revenues
from acquisitions |
|
(31,008 |
) |
|
— |
|
|
Less contribution of revenues
from divested products |
|
— |
|
|
(13 |
) |
|
Total organic revenues(1) |
$ |
349,642 |
|
$ |
382,408 |
|
(8.6 |
)% |
|
|
|
|
Boston Revenue impact |
$ |
(779 |
) |
$ |
6,389 |
|
|
Total organic revenues(1) excl. Boston |
$ |
348,863 |
|
$ |
388,797 |
|
(10.3 |
)% |
|
(1) Organic revenues have been adjusted to exclude foreign
currency (current period), acquisitions and to account for divested
and discontinued products.(2) Prior period revenues included within
our instruments business have been reclassified under the ENT
business.
Items included in GAAP net income and location where each item
is recorded are as follows:
(In thousands) |
Three Months Ended September 30, 2024 |
Item |
Total Amount |
COGS(a) |
SG&A(b) |
R&D(c) |
Amort (d) |
OI&E(e) |
Tax(f) |
Acquisition, divestiture and integration-related charges |
7,810 |
|
3,643 |
5,896 |
(1,712 |
) |
— |
(17 |
) |
— |
|
Structural Optimization
charges |
5,739 |
|
3,737 |
1,983 |
19 |
|
— |
— |
|
— |
|
EU Medical Device Regulation
charges |
10,578 |
|
823 |
4,844 |
4,910 |
|
— |
— |
|
— |
|
Boston Recall/Braintree
Transition |
9,933 |
|
9,601 |
333 |
— |
|
— |
— |
|
— |
|
Intangible asset amortization
expense |
25,615 |
|
21,854 |
— |
— |
|
3,761 |
— |
|
— |
|
Estimated income tax impact
from above adjustments and other items |
(17,244 |
) |
— |
— |
— |
|
— |
— |
|
(17,244 |
) |
Depreciation expense |
10,216 |
|
— |
— |
— |
|
— |
— |
|
— |
|
|
|
|
|
|
|
|
|
a) COGS - Cost of goods soldb)
SG&A - Selling, general and administrativec) R&D - Research
& developmentd) Amort. - Intangible asset amortizatione)
OI&E - Other income & expensef) Tax - Income tax expense
(benefit)
Items included in GAAP net income and location where each item
is recorded are as follows:
(In thousands) |
Three Months Ended September 30, 2023 |
Item |
Total Amount |
COGS(a) |
SG&A(b) |
R&D(c) |
Amort (d) |
OI&E(e) |
Tax(f) |
Acquisition, divestiture and integration-related charges |
5,832 |
|
407 |
6,638 |
(1,090 |
) |
— |
(123 |
) |
— |
|
Structural Optimization
charges |
3,729 |
|
1,847 |
1,909 |
(27 |
) |
— |
— |
|
— |
|
EU Medical Device Regulation
charges |
13,490 |
|
1,263 |
5,661 |
6,565 |
|
— |
— |
|
— |
|
Boston Recall |
7,800 |
|
7,706 |
94 |
— |
|
— |
— |
|
— |
|
Intangible asset amortization
expense |
20,869 |
|
17,661 |
— |
— |
|
3,208 |
— |
|
— |
|
Estimated income tax impact
from above adjustments and other items |
(10,677 |
) |
— |
— |
— |
|
— |
— |
|
(10,677 |
) |
Depreciation expense |
9,670 |
|
— |
— |
— |
|
— |
— |
|
— |
|
|
a) COGS - Cost of goods soldb)
SG&A - Selling, general and administrativec) R&D - Research
& developmentd) Amort. - Intangible asset amortizatione)
OI&E - Other income & expensef) Tax - Income tax expense
(benefit)
|
RECONCILIATION OF NON-GAAP ADJUSTMENTS - GAAP NET INCOME TO
ADJUSTED EBITDA(UNAUDITED) |
(In
thousands) |
|
Three Months Ended September 30, |
|
|
2024 |
|
|
|
2023 |
|
|
|
|
|
GAAP net income (loss) |
$ |
(10,695 |
) |
|
$ |
19,497 |
|
Non-GAAP adjustments: |
|
|
|
Depreciation and intangible
asset amortization expense |
|
35,831 |
|
|
|
30,538 |
|
Other (income) expense,
net |
|
(2,095 |
) |
|
|
(348 |
) |
Interest expense, net |
|
14,324 |
|
|
|
8,455 |
|
Income tax expense |
|
(9,667 |
) |
|
|
(888 |
) |
Structural optimization
charges |
|
5,739 |
|
|
|
3,729 |
|
EU Medical Device Regulation
charges |
|
10,578 |
|
|
|
13,490 |
|
Boston Recall/ Braintree
transition |
|
9,933 |
|
|
|
7,800 |
|
Acquisition, divestiture and
integration-related charges(1) |
|
7,810 |
|
|
|
5,832 |
|
Total of non-GAAP
adjustments |
|
72,453 |
|
|
|
68,608 |
|
Adjusted EBITDA |
$ |
61,758 |
|
|
$ |
88,105 |
|
|
|
|
|
RECONCILIATION OF NON-GAAP ADJUSTMENTS - GAAP NET INCOME TO
MEASURES OF ADJUSTED NET INCOME AND ADJUSTED EARNINGS PER
SHARE(UNAUDITED) |
(In thousands, except per share amounts) |
|
|
Three Months Ended September 30, |
|
|
2024 |
|
|
|
2023 |
|
|
|
|
|
GAAP net income (loss) |
$ |
(10,695 |
) |
|
$ |
19,497 |
|
Non-GAAP adjustments: |
|
|
|
Structural optimization
charges |
|
5,739 |
|
|
|
3,729 |
|
Acquisition, divestiture and
integration-related charges |
|
7,810 |
|
|
|
5,832 |
|
EU Medical Device Regulation
charges |
|
10,578 |
|
|
|
13,490 |
|
Boston Recall/Braintree
Transition |
|
9,933 |
|
|
|
7,800 |
|
Intangible asset amortization
expense |
|
25,615 |
|
|
|
20,869 |
|
Estimated income tax impact
from adjustments and other items |
|
(17,244 |
) |
|
|
(10,677 |
) |
Total of non-GAAP
adjustments |
|
42,431 |
|
|
|
41,042 |
|
Adjusted net income |
$ |
31,736 |
|
|
$ |
60,539 |
|
|
|
|
|
Adjusted diluted net income
per share |
$ |
0.41 |
|
|
$ |
0.76 |
|
Weighted average common shares
outstanding for diluted net income per share |
|
76,478 |
|
|
|
79,811 |
|
|
CONDENSED BALANCE SHEET DATA(UNAUDITED) |
(In thousands) |
|
|
September 30,2024 |
|
|
December 31,2023 |
|
|
|
|
|
Short term investments |
$ |
62,441 |
|
|
$ |
32,694 |
|
Cash and cash equivalents |
|
215,157 |
|
|
|
276,402 |
|
Trade accounts receivable,
net |
|
248,298 |
|
|
|
259,327 |
|
Inventories, net |
|
436,930 |
|
|
|
389,608 |
|
|
|
|
|
|
Current and long-term
borrowing under senior credit facility |
|
1,161,355 |
|
|
|
840,094 |
|
Borrowings under
securitization facility |
|
72,800 |
|
|
|
89,200 |
|
Convertible securities |
|
572,442 |
|
|
|
570,255 |
|
|
|
|
|
|
|
|
|
|
|
Stockholders' equity |
$ |
1,521,587 |
|
|
$ |
1,587,884 |
|
|
|
|
|
|
|
|
|
|
|
CONDENSED STATEMENT OF CASH FLOWS(UNAUDITED) |
(In thousands) |
|
|
Nine Months Ended September 30, |
|
|
2024 |
|
|
|
2023 |
|
|
|
|
|
Net cash provided by operating
activities |
$ |
78,642 |
|
|
$ |
81,205 |
|
Net cash used in investing
activities |
|
(386,559 |
) |
|
|
(36,949 |
) |
Net cash provided by (used by)
by financing activities |
|
245,013 |
|
|
|
(223,035 |
) |
Effect of exchange rate
changes on cash and cash equivalents |
|
1,659 |
|
|
|
(4,150 |
) |
|
|
|
|
Net decrease in cash and cash
equivalents |
$ |
(61,245 |
) |
|
$ |
(182,929 |
) |
|
|
|
|
RECONCILIATION OF NON-GAAP ADJUSTMENTS - GAAP OPERATING CASH FLOW
TO MEASURES OF FREE CASH FLOW AND ADJUSTED FREE CASH FLOW
CONVERSION(UNAUDITED) |
(In thousands) |
|
|
Three Months Ended September 30, |
|
|
2024 |
|
|
2023 |
|
Net cash provided by operating
activities |
$ |
22,480 |
|
$ |
26,770 |
|
|
|
|
|
|
|
Purchases of property and
equipment |
$ |
(29,646 |
) |
$ |
(13,062 |
) |
Free cash flow |
|
(7,166 |
) |
|
13,708 |
|
|
|
|
Adjusted net income(1) |
$ |
31,736 |
|
$ |
60,539 |
|
Adjusted free cash flow
conversion |
(22.6 |
)% |
|
22.6 |
% |
|
|
|
|
|
|
|
|
|
|
Twelve Months Ended September 30, |
|
|
2024 |
|
|
2023 |
|
Net cash provided by operating
activities |
$ |
137,385 |
|
$ |
166,538 |
|
|
|
|
Purchases of property and
equipment |
|
(99,381 |
) |
|
(56,868 |
) |
Free cash flow |
$ |
38,004 |
|
$ |
109,670 |
|
|
|
|
Adjusted net income(1) |
$ |
192,791 |
|
$ |
257,514 |
|
Adjusted free cash flow
conversion |
|
19.7 |
% |
|
42.6 |
% |
|
|
|
(1) Adjusted net income for quarters ended September 30, 2024
and 2023 are reconciled above. Adjusted net income for remaining
quarters in the trailing twelve months calculation have been
previously reconciled and are publicly available in the Quarterly
Earnings Call Presentations on our website at
investor.integralife.com under Events & Presentations.
The Company calculates adjusted free cash flow conversion by
dividing its free cash flow by adjusted net income. The Company
believes this measure is useful in evaluating the significance of
the cash special charges in its adjusted earnings measures.
|
RECONCILIATION OF NON-GAAP ADJUSTMENTS - NET DEBT
CALCULATION(UNAUDITED) |
|
(In thousands) |
|
|
September 30,2024 |
December 31,2023 |
Short-term borrowings under senior credit facility |
|
29,063 |
|
|
14,531 |
|
Long-term borrowings under
senior credit facility |
|
1,132,292 |
|
|
825,563 |
|
Borrowings under
securitization facility |
|
72,800 |
|
|
89,200 |
|
Convertible securities |
|
572,442 |
|
|
570,255 |
|
Deferred financing costs
netted in the above |
|
6,516 |
|
|
9,651 |
|
Short term investments |
|
(62,441 |
) |
|
(32,694 |
) |
Cash & Cash
Equivalents |
|
(215,157 |
) |
|
(276,402 |
) |
Net Debt |
$ |
1,535,515 |
|
$ |
1,200,104 |
|
|
|
|
RECONCILIATION OF NON-GAAP ADJUSTMENTS - GAAP GROSS PROFIT TO
MEASURES OF ADJUSTED GROSS PROFIT AND ADJUSTED GROSS
MARGIN(UNAUDITED) |
(In thousands, except percentages) |
|
|
Three Months Ended September 30, |
|
|
2024 |
|
|
|
2023 |
|
|
|
|
|
Total revenues, net |
$ |
380,834 |
|
|
$ |
382,421 |
|
Cost of goods sold |
|
180,596 |
|
|
|
164,076 |
|
Reported Gross Profit |
|
200,238 |
|
|
|
218,345 |
|
Structural optimization
charges |
|
3,737 |
|
|
|
1,847 |
|
Acquisition, divestiture and
integration-related charges |
|
3,643 |
|
|
|
407 |
|
Boston Recall/Braintree
Transition |
|
9,601 |
|
|
|
7,706 |
|
EU Medical Device
Regulation |
|
823 |
|
|
|
1,263 |
|
Intangible asset amortization
expense |
|
21,854 |
|
|
|
17,661 |
|
Adjusted Gross Profit |
$ |
239,895 |
|
|
$ |
247,229 |
|
Total Revenues |
$ |
380,834 |
|
|
$ |
382,421 |
|
Adjusted Gross Margin |
|
63.0 |
% |
|
|
64.6 |
% |
Integra LifeSciences (NASDAQ:IART)
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Integra LifeSciences (NASDAQ:IART)
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From Jan 2024 to Jan 2025