Earnings summaries and quarterly performance for Penumbra.
Executive leadership at Penumbra.
Board of directors at Penumbra.
Research analysts who have asked questions during Penumbra earnings calls.
Richard Newitter
Truist Securities
4 questions for PEN
Robert Marcus
JPMorgan Chase & Co.
4 questions for PEN
Macauley Kilbane
William Blair & Company
3 questions for PEN
Michael Sarcone
Jefferies
3 questions for PEN
Pito Chickering
Deutsche Bank
3 questions for PEN
Ryan Zimmerman
BTIG
3 questions for PEN
Joanne Wuensch
Citigroup Inc.
2 questions for PEN
Lei Huang
Wells Fargo
2 questions for PEN
Michael Kratky
Leerink Partners
2 questions for PEN
Samantha Kurtz
Piper Sandler Companies
2 questions for PEN
Travis Steed
Bank of America
2 questions for PEN
William Plovanic
Canaccord Genuity
2 questions for PEN
Bill Plovanic
Canaccord Genuity
1 question for PEN
Brandon Vazquez
William Blair & Company, L.L.C.
1 question for PEN
Chris Pasquale
Nephron Research LLC
1 question for PEN
Christopher Pasquale
Nephron Research
1 question for PEN
David Rescott
Baird
1 question for PEN
Kallum Titchmarsh
Morgan Stanley
1 question for PEN
Larry Biegelsen
Wells Fargo & Company
1 question for PEN
Lawrence Biegelsen
Wells Fargo
1 question for PEN
Mathew Blackman
Stifel
1 question for PEN
Matthew O'Brien
Piper Sandler & Co.
1 question for PEN
Michael Matson
Needham & Company
1 question for PEN
Samantha Munoz
Piper Sandler Companies
1 question for PEN
Shagun Singh Chadha
RBC Capital Markets
1 question for PEN
Recent press releases and 8-K filings for PEN.
- Penumbra, Inc. reported revenue of $385.4 million for the fourth quarter of 2025, an increase of 22.1% compared to the fourth quarter of 2024, and full year 2025 revenue of $1,403.7 million, an increase of 17.5% compared to full year 2024.
- Net income for Q4 2025 was $47.3 million and for the full year 2025 was $177.7 million.
- Income from operations reached $59.2 million (15.4% operating margin) in Q4 2025 and $189.2 million (13.5% operating margin) for the full year 2025.
- The company will not provide financial guidance for full year 2026 due to a proposed acquisition by Boston Scientific Corporation.
- Penumbra, Inc. reported revenue of $385.4 million for the fourth quarter of 2025, an increase of 22.1% compared to Q4 2024, and $1,403.7 million for the full year 2025, up 17.5% from FY 2024.
- Net income was $47.3 million for the fourth quarter of 2025 and $177.7 million for the full year 2025.
- Adjusted EBITDA reached $79.1 million in the fourth quarter of 2025 and $266.8 million for the full year 2025.
- The company will not provide financial guidance for the full year 2026 due to a proposed acquisition by Boston Scientific Corporation.
- Penumbra, Inc. is being acquired by Boston Scientific Corporation in a cash and stock transaction valued at $374 per share, reflecting an enterprise value of approximately $14.5 billion.
- The transaction consideration will be approximately 73% cash and 27% Boston Scientific common stock, with Penumbra stockholders having the right to elect their preferred form of consideration.
- For the fourth quarter of 2025, Penumbra reported preliminary revenue between $383.0 million and $384.8 million, representing growth of approximately 21.4% to 22.0% compared to Q4 2024.
- For the full year 2025, preliminary revenue was between $1,401.3 million and $1,403.1 million, an increase of approximately 17.3% to 17.5% over the prior fiscal year.
- Preliminary Q4 2025 gross margin was 67.9% to 68.1%, with income from operations ranging from $56.9 million to $60.4 million.
- Penumbra, Inc. announced preliminary fourth quarter 2025 revenue between $383.0 million and $384.8 million, reflecting growth of approximately 21.4% to 22.0% compared to the fourth quarter of 2024.
- For the full year 2025, preliminary revenue is estimated to be between $1,401.3 million and $1,403.1 million, representing growth of approximately 17.3% to 17.5% compared to the full year 2024.
- The company reported preliminary gross margin of 67.9% to 68.1% for the fourth quarter 2025 and 67.1% for the full year 2025.
- Preliminary income from operations for the fourth quarter 2025 was $56.9 million to $60.4 million, with an operating margin of 14.8% to 15.7%.
- Penumbra is expanding its manufacturing capabilities with a new facility in Costa Rica scheduled to open in mid to late 2027.
- The company's Thunderbolt computer-assisted vacuum thrombectomy (CAVT) product is currently under FDA submission, with the company having addressed follow-up questions.
- The STORM-PE trial demonstrated statistically significant positive outcomes for Penumbra's CAVT arm in pulmonary embolism treatment, including a reduction in RV/LV ratio and strong safety, with procedure times as low as 25 minutes.
- The embolization business, particularly for MMA (middle meningeal artery) embolization with the Swift Coil, has become a significant growth driver, achieving over 100% growth in recent quarters.
- Penumbra aims to exit 2026 with 70%+ margins.
- Penumbra is expanding its manufacturing capabilities with a new 330,000 sq ft facility in Costa Rica slated to open in mid-to-late 2027, complementing its existing California operations.
- The company's thrombectomy business is seeing strong results, particularly from the STORM-PE trial for pulmonary embolism, which showed statistically significant improvements and excellent safety, while its neuro thrombectomy product, Thunderbolt, is currently under FDA submission.
- Penumbra's embolization business is a significant growth driver, with its coil business achieving over 100% growth in recent quarters, boosted by a new coil launch and the emerging opportunity in Middle Meningeal Artery (MMA) embolization.
- The company is committed to achieving 70%+ margins by the end of 2026, driven by operational efficiencies and strategic market adjustments.
- Penumbra, Inc. is headquartered in Alameda, has approximately 4,500 employees, and its products are available in 100+ markets.
- The company is expanding its manufacturing capabilities with a new 330,000 square foot facility in Costa Rica that is due to open in mid-2027.
- Penumbra highlighted a total annual U.S. market opportunity of over 1,250,000 patients for its thrombectomy products and market opportunities including 175,000 peripheral procedures and 140,000 MMAe patients for embolization.
- The STORM-PE RCT demonstrated that the CAVT arm achieved a significantly greater reduction in right heart strain (29.7% relative reduction) compared to the AC arm, with a comparable safety profile and 100% technical success.
- Penumbra is expanding its manufacturing capabilities with a new 330,000 sq ft facility in Costa Rica scheduled to open in mid to late 2027, which is expected to support the production of more cost-effective products.
- The company highlights significant growth in both its thrombectomy and embolization businesses, with the latter seeing over 100% growth in recent quarters, particularly from the Middle Meningeal Artery (MMA) opportunity.
- The Thunderbolt neuro product is currently 9 months into its FDA submission process, with the company addressing follow-up questions.
- Penumbra is committed to achieving over 70% margins by the end of 2026 and anticipates that China will no longer be a growth headwind in 2026.
- Penumbra reported strong Q3 performance in its MO and access business, driven by the launch of Ruby XL and the expansion of its sales force.
- The company highlighted a significant growth opportunity in MMA embolization on the neuro side, with a potential $1 billion opportunity for this new procedure.
- Results from the STORM-PE trial demonstrated that mechanical thrombectomy with CAVT is superior to anticoagulation for pulmonary embolism treatment, showing high safety and fast procedure times (25-minute device time, 56-minute procedure time), which is expected to drive increased market penetration.
- Penumbra introduced 3.0, an updated product with both software and hardware changes, offering faster operation and less blood loss compared to its predecessor.
- The FDA review process for the Thunderbolt product is described as thorough but routine, with the company addressing clarifying questions.
- Penumbra reported strong performance in its MO and access business in Q3, driven by a new sales force and the successful launch of Ruby XL, a large vessel coil for peripheral vascular embolization.
- The company is experiencing significant growth in neuro embolization, particularly from the new MMA embolization procedure, which is seen as a potential $1 billion opportunity.
- The STORM-PE study demonstrated that Penumbra's mechanical thrombectomy with CAVT is superior to anticoagulation for pulmonary embolism, showing extraordinary safety, significant RV/LV ratio reduction, and rapid procedure times. This data is influencing hospital protocols and expanding market penetration.
- Penumbra introduced 3.0, an enhanced thrombectomy product that offers faster operation and reduced blood loss, and is currently navigating the FDA review process for its Thunderbolt product, which is expected to have a higher average selling price.
Quarterly earnings call transcripts for Penumbra.
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