
Third Quarter 2026 Earnings Conference Call
11/5/2026
Conference Call LogisticsThe release, accompanying slides, and replay webcast are available online at https://www.teleflex.com (click on Investors)
An audio replay of the call will be available beginning at 11:00 am Eastern Time on November 5, 2026 either on the Teleflex website or by telephone.
The call can be accessed by dialing
1 833 309 1852 (U.S. and Canada) or 1 929 828
5978
(all other locations).
The confirmation code is 893 259 060.
Today's Speakers Jason WeidmanPresident and CEO
John DerenExecutive VP and CFO
Lawrence Keusch VP, Investor Relations and Strategy DevelopmentTELEFLEX EARNINGS CONFERENCE CALL 11/5/2026
Note on Forward-Looking StatementsThis presentation contains forward-looking statements, including, but not limited to, our forecasted 2026: GAAP, pro forma adjusted revenue and pro forma adjusted constant currency revenue growth, GAAP and adjusted operating margin and GAAP and adjusted earnings per share and, in each case, our estimates with respect to the items expected to impact those forecasted results; statements regarding our planned uses of the net proceeds from the closing of the sale of our OEM business (the "OEM Strategic Divestiture"), including, without limitation, with respect to the paydown of debt and the repurchase of shares of our outstanding common stock; statements regarding our expectations with respect to the timing for closing of the sales of our Acute Care and Interventional Urology businesses (which, together with the OEM Strategic Divestiture, we refer to as the "Strategic Divestitures"); statements regarding projected costs, savings and timing with respect to restructuring activities related to the Strategic Divestitures; our expectation that the transition services and manufacturing services agreements to be entered into in connection with the Strategic Divestitures will offset stranded costs on an annualized basis; statements regarding EZPLAZ; statements regarding our BIOMAG-II and BIOMAG-III trials and our BIOMAG-LL clinical study; our expectation that our financial profile will be meaningfully stronger starting in 2027; and other matters which inherently involve risks and uncertainties which could cause actual results to differ from those projected or implied in the forward-looking statements. Any forward-looking statements contained herein are based on our management's current beliefs and expectations, but are subject to a number of risks, uncertainties and changes in circumstances, which may cause actual results or company actions to differ materially from what is expressed or implied by these statements. These risks and uncertainties are identified and described in more detail in our filings with the Securities and Exchange Commission, including our Annual Report on Form 10-K. We expressly disclaim any obligation to update these forward-looking statements, except as otherwise explicitly stated by us or as required by law or regulation. You should not place undue reliance on these statements or the scientific data presented.
Note on Non-GAAP Financial MeasuresThis presentation refers to certain non-GAAP financial measures, including, but not limited to, pro forma adjusted revenue, pro forma adjusted constant currency revenue growth, adjusted diluted earnings per share, adjusted gross and operating margins, adjusted selling, general and administrative expenses, adjusted research and development expenses, adjusted income before taxes, adjusted income tax expense and adjusted tax rate. These non-GAAP financial measures should not be considered replacements for, and should be read together with, the most comparable GAAP financial measures. Tables reconciling these non-GAAP financial measures to the most comparable GAAP financial measures are contained within this presentation and the appendices at the end of this presentation.
Additional NotesThis document contains certain highlights with respect to our third quarter 2026 results and developments and does not purport to be a complete summary thereof. Accordingly, we encourage you to read our Earnings Release for the quarter ended September 30, 2026 located in the investor section of our website at https://www.teleflex.com and our Quarterly Report on Form 10-Q for the quarter ended September 30, 2026 to be filed with the Securities and Exchange Commission.
Unless otherwise noted, the following slides reflect continuing operations.
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Executive OverviewJason Weidman President and CEO
Q3'26 Highlights Q3 Performance SummaryQ3'26 pro forma adjusted constant currency revenue grew 3.0%
year-over-year
Q3'26 adjusted gross margin of 66.8% and adjusted operating margin of 25.0%
Q3'26 adjusted EPS of $2.63, a 39.2% increase year-over-year
OEM Divestiture Update
Closed the OEM Strategic Divestiture for $1.5 billion in proceeds ($1.25 billion after-tax)
OEM Strategic Divestiture generates the majority of our expected
and
proceeds from the Strategic Divestitures - funded debt paydown
share repurchase
Note: See tables appearing in this presentation and the appendices hereto for reconciliations of non-GAAP financial information.
TELEFLEX EARNINGS CONFERENCE CALL 11/5/2026
Innovation UpdatesEZPLAZTM: Building a Long-Term Growth Driver
Q3 2026 UPDATE
EZPLAZTM
Freeze Dried Plasma
At Least $200 Million
potential long-term U.S. market opportunity and a meaningful growth driver for Teleflex
First and only FDA-licensed freeze dried plasma; approved in late July; customer interest has been high
Stored at room temperature and ready to reconstitute in minutes - makes plasma available on the battlefield, in air and road ambulances, and in trauma centers without waiting to thaw1,2
Flexible bag is a meaningful differentiator vs. glass-container formats expected from future entrants; first-mover advantage positions EZPLAZ to set the standard
Initial priority is the U.S. government and military, expected to account for the majority of current manufacturing capacity; Department of War discussions continue to progress
EXPECTED REVENUE PROFILE
2026
Immaterial revenue
2027
Revenue contributor
Beyond 2027
Modest ramp over the first several years as the market is built and supply scales
Pusateri AE, Given MB, Schreiber MA, et al. Dried plasma: state of the science and recent developments. Transfusion. 2016;56 Suppl 2:S128-S139. doi:10.1111/ trf.13580
Hervig T, Doughty H, Ness P, et al. Prehospital use of plasma: the blood bankers' perspective. Shock. 2014;41 Suppl 1:39-43. doi:10.1097/SHK.0000000000000144
Rx Only
See appendices to this presentation for EZPLAZ™ Freeze Dried Plasma Indications and Important Safety Information.
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Innovation UpdatesDifferentiated
Freesolve combines temporary scaffolding with drug delivery to target rapidly growing interventional trend to "leave nothing behind"
Late-2027
BIOMAG-II: first randomized clinical data readout expected
FreesolveTM Resorbable Magnesium Scaffold (RMS) Breakthrough Device Designation Received
Received FDA Breakthrough Device Designation (BDD) for FreesolveTM RMS in percutaneous coronary intervention (PCI), building on the 2024 BDD for below-the-knee (BTK) treatment of chronic limb-ischemia
BIOMAGTM-II: enrollment completed ahead of schedule; one-year data vs. XIENCETM Drug-Eluting Stent (DES) expected in late 2027
BIOMAGTM-III: U.S. pivotal trial underway to support a future Premarket Approval (PMA) submission
BIOMAGTM-LL Clinical Study Enrollment Completed
Completed enrollment of 102 patients across 14 European centers evaluating 35 mm and 40 mm FreesolveTM RMS lengths in de novo coronary lesions up to 38 mm
Primary endpoint is 12-month target lesion failure (TLF)*
Study will help determine whether longer scaffold lengths may enable treatment of long lesions with fewer implants, potentially simplifying procedures and reducing scaffold overlap
35 mm and 40 mm lengths are also included in the ongoing BIOMAGTM-III pivotal clinical trial
*Target lesion failure (TLF) is a composite clinical endpoint commonly used to assess the safety and effectiveness of coronary interventional devices.
CAUTION-Investigational device. Limited by the United States law to investigational use.
FreesolveTM RMS is not for sale in the United States and is commercially available in CE-mark accepting countries only. Indications for Use may vary by geographic location.
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Q3'26 Segment Commentary of Continuing OperationsSales ($M) Commentary
Vascular
$243.5
Reported rev. growth: 4.7% Pro forma adj. const. curr. rev. growth: 4.6%
In Q3'26, growth was primarily driven by our intraosseous portfolio, hemostatic products, and peripheral access products
As expected, saw some distributor inventory destocking associated with normalization following the lidocaine recall earlier in the year
Interventional
$210.3
Reported rev. growth: (2.6)% Pro forma adj. const. curr. rev. growth: 0.2%
Surgical
$114.0
Reported rev. growth: 4.2% Pro forma adj. const. curr. rev. growth: 5.1%
While several categories including complex catheters, hemostatic products, right heart catheters, and OnControl outperformed, growth was impacted by the ongoing integration and restructuring activities associated with the VI acquisition
Made good progress in Q3'26 on the mitigation actions addressing the temporary integration dynamics previously communicated; new leadership in place
Q3'26 growth was primarily driven by strong performances in ligation clips and skin stapling
As expected, growth remained strong but moderated from the first half due to the challenging comparison from the acceleration of our new instrument portfolio in mid-2025
Note: See tables appearing in this presentation and the appendices hereto for reconciliations of non-GAAP financial information. Pro forma adjusted constant currency revenue growth is as compared to the prior year period.
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Q3'26 Revenue Review By SegmentReported Revenue | September 30, 2026 Adjustment | Pro Forma Adjusted Revenue | Reported Revenue | September 28, 2025 Adjustment | Pro Forma Adjusted Revenue | Reported Revenue Growth | % Increase / (Decrease) Currency Impact Adjustment Impact | Pro Forma Adjusted Constant Currency Revenue Growth | ||
Vascular | $243.5 | $- | $243.5 | $232.5 | $- | $232.5 | 4.7% | 0.1% | -% | 4.6% |
Interventional1 | 210.3 | - | 210.3 | 215.9 | (5.0) | 210.9 | (2.6)% | (0.5)% | (2.3)% | 0.2% |
Surgical2 | 114.0 | - | 114.0 | 109.5 | (0.7) | 108.8 | 4.2% | (0.3)% | (0.6)% | 5.1% |
Segment Net Revenues1 | 567.8 | - | 567.8 | 557.9 | (5.7) | 552.2 | 1.8% | (0.2)% | (1.0)% | 3.0% |
Other3 | - | - | - | 9.0 | (9.0) | - | (100.0)% | -% | (100.0)% | -% |
Consolidated Net Revenues1 | $567.8 | $- | $567.8 | $566.9 | $(14.7) | $552.2 | 0.2% | (0.2)% | (2.6)% | 3.0% |
Three Months Ended September 30, 2026
Note: See tables appearing in this presentation and the appendices hereto for reconciliations of non-GAAP financial information.
Adjustments are inclusive of Vascular Intervention pro forma and discontinued product adjustments
Adjustments are inclusive of discontinued product adjustments
In 2025, amounts reflect the impact from decreases in our reserves related to the Italian payback measure pertaining to prior years.
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Financial OverviewJohn Deren
Executive VP and CFO
Q3'26 Financial Review of Continuing OperationsAdjusted GAAP
2025 62.3%
450
bps
2026 66.8%
2025 32.7%
2026 34.3%
2025 7.6%
2026 7.5%
2025 22.0%
300
bps
2026 25.0%
2025 $1.89
2026 $2.63
2025 51.5%
2026 65.0%
2025 36.6%
2026 38.9%
2025 7.8%
2026 7.6%
Gross Margin
The year-over-year adjusted gross margin increase was primarily driven by the following:
a 290 bps benefit from a refund related to 2026 IEEPA tariff payments
and foreign currency fluctuations, partially offset by an increase in quality remediation charges
SG&A Expense
(% of Sales)
The year-over-year adjusted SG&A expense % of sales increase was driven by the following:
operating expenses associated with business and employee investments
R&D Expense
(% of Sales)
Year-over-year adjusted R&D expense % of sales was flat
Operating Margin
2025 (11.0)%
2026 18.6%
The year-over-year adjusted operating margin increase was driven by the following:
year-over-year gross margin increase
Earnings per Share
partially offset by business investments and higher incentive compensation (stronger performance in 2026 and lower prior year accrual)
Note: See appendices for reconciliations of non-GAAP financial information.
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2025
-$1.32
$1.30
2026
The year-over-year adjusted earnings per share increase was driven by the following:
higher sales volume, lower interest expense and shares outstanding, and tariff refunds
Capital Allocation Strategy UpdateCapital return commitment
$1 billion share repurchase authorization and $800 million reduction in debt
Near-term capital return to shareholders to be primarily funded by after-tax proceeds from the Strategic Divestitures
Share repurchases
From July 1, 2026 through the date of this presentation, the Company has repurchased $350 million of its common stock through an ASR program ($250 million) and open market purchases ($100 million)
This consisted of 2.7 million shares repurchased at an average price of $128.96 per share
As of November 5, 2026, the Company had $400 million remaining available under the current authorization
TELEFLEX EARNINGS CONFERENCE CALL 11/5/2026 13
2026 Financial Guidance RevenueMaintaining 2026 pro forma adjusted constant currency revenue growth range of 3.5% to 4.5% year-over-year
Reducing 2026 GAAP revenue from continuing operations growth range to 13.2% to 14.2% year-over-year due to changes in foreign currency exchange rates
Earnings Per Share
Increasing 2026 Adjusted diluted EPS from continuing operations range to $7.50 to $7.75
Increasing 2026 GAAP EPS from continuing operations range to $2.84 to $3.09
Note: See tables appearing in this presentation and the appendices hereto for reconciliations of non-GAAP financial information. TELEFLEX EARNINGS CONFERENCE CALL 11/5/2026 14
2026 Guidance Considerations3.5% to 4.5% pro forma adjusted constant currency revenue growth for 2026
Pro Forma Adj. CC Revenue Growth
Excludes foreign exchange, Italian payback measure, and discontinued products
Includes Vascular Intervention revenue for the first half of 2025
Adjusted Earnings Per Share2026 adjusted EPS from continuing operations in the range of $7.50 to $7.75
Assumes:
~20.0% adjusted operating margin inclusive of IEEPA tariff refunds of $16.5M recognized in the third quarter 2026
~11.5% adjusted tax rate
$85M of net interest expense
42.5 million shares outstanding for 2026
Reflects execution of capital allocation strategy, including pay off of $700 million Term Loan A-2, pay down of a portion of the revolving credit facility, and $600 million of share repurchases
Excludes transition services (TS) and manufacturing services (MS) benefits from the Acute Care & Interventional Urology Strategic Divestiture
Excludes future repurchases under the $1B buyback program funded by Strategic Divestitures proceeds, of which $400 million is remaining
Excludes incremental debt paydown with net proceeds from the Strategic Divestitures
Note: See tables appearing in this presentation and the appendices hereto for reconciliations of non-GAAP financial information.
TELEFLEX EARNINGS CONFERENCE CALL 11/5/2026 15
2026 Financial Guidance - Future OpportunitiesAdjusted Operating Margin
TS/MS agreements expected to offset stranded costs on an annualized basis following close of AC/IU Strategic Divestiture
Previously announced restructuring programs to result in ~$50 million of pre-tax savings on an annualized basis upon completion in mid-2028, which will contribute to mitigating stranded costs
Debt Paydown
Intent to pay down ~$800M in debt (paid off $700 million of debt associated with the Vascular Intervention acquisition), with net proceeds from the Strategic Divestitures
Share Repurchase
Remaining $400 million authorization under previously announced share repurchase program to be funded with net proceeds from the Strategic Divestitures
Working on additional cost savings to further mitigate stranded costs
TELEFLEX EARNINGS CONFERENCE CALL 11/5/2026 16
2026 Financial Guidance of Continuing Operations Summary2026 Guidance | Low | High |
GAAP Revenue Growth | 13.2% | 14.2% |
Impact of Vascular Intervention Pro Forma | 10.0% 10.0% | |
Impact of Discontinued Product | (0.7)% | (0.7)% |
Impact of Italian Payback Measure | (0.5)% (0.5)% | |
Base Year Adjustment (GAAP Versus Pro Forma Adjusted) | 0.4% | 0.4% |
Impact of Foreign Exchange Rate Fluctuations | 0.5% 0.5% | |
Pro Forma Adjusted Constant Currency Revenue Growth | 3.5% | 4.5% |
Adjusted Operating Margin | ~20.0% | |
Adjusted EPS | $7.50 | $7.75 |
Adjusted EPS % Growth | 7.4% | 11.0% |
Note: See appendices for reconciliations of non-GAAP financial information.
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Forecasted 2026 Pro Forma Adjusted Revenue From Continuing Operations Reconciliation2026 Guidance | 2025 | 2026 Guidance | |
Low | High | ||
GAAP revenue | $1,992.7 $2,256 | $2,276 | |
Vascular Intervention pro forma adjustment | 199.0 - | - | |
Discontinued product adjustment | (14.3) - | - | |
Italian payback measure adjustment | (9.0) - | - | |
Pro forma adjusted revenue | $2,168.4 $2,256 | $2,276 | |
Note: See appendices for reconciliations of non-GAAP financial information.
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Key TakeawaysStrong Q3 Performance; Raising FY26 Adjusted EPS Guidance
Expanded adj. margins; grew adj. EPS
Vascular & Surgical solid; Interventional moving in the right direction
Maintaining FY26 revenue growth outlook
Meaningful Progress on Our Transformation
Interventional integration advancing with new leadership in place
Confident in completing the AC/IU divestiture
Advancing longer-term growth with EZPLAZ and Freesolve
Clear Path to a Meaningful Step-Up in 2027+
Priorities: strengthen foundation, accelerate organizational effectiveness, elevate growth profile
Planned completion of $1B buyback after AC/IU close
2027 step-up in adj. op. margin & EPS; sustainable growth beyond
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Thank You!
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