Focus: Penumbra is a public medical device company specializing in minimally-invasive vascular and surgical devices for acute stroke, pulmonary embolism, and intracranial hemorrhage. The company operates at ~$1.1B in FY2025 revenue with strong recent growth and profitability.
Profile data last refreshed 11h ago · AI intelligence enriched 1mo ago
Growing — net +11 jobs in 30d
43 jobs added vs 32 removed. Steady team buildout.
Best suited for commercial, operational, and manufacturing professionals seeking growth in a profitable, acquisition-target medical device company; limited appeal for pure research scientists.
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
Generated by Claude from Penumbra's SEC filings, pipeline programs, hiring velocity, FDA actions, and WARN data. Inference, not editorial — verify before quoting.
Automated analysis based on publicly available data (FDA, SEC, ClinicalTrials.gov). May be incomplete or delayed. This score does not reflect insider knowledge and should not be used as the sole basis for investment or employment decisions.
Penumbra (PEN) Starts The FORWARD Study, Is The Stock Already Expensive? - simplywall.st
Penumbra (PEN) Starts The FORWARD Study, Is The Stock Already Expensive? simplywall.st
Penumbra wins CE mark for Thunderbolt clot removal tech - MedTech Dive
Penumbra wins CE mark for Thunderbolt clot removal tech MedTech Dive
CE Mark Granted to Penumbra's CAVT Platform - dicardiology.com
CE Mark Granted to Penumbra's CAVT Platform dicardiology.com
Penumbra Expands CAVT for Stroke to Europe with CE Mark for THUNDERBOLT - PR Newswire
Penumbra Expands CAVT for Stroke to Europe with CE Mark for THUNDERBOLT PR Newswire
Penumbra Expands CAVT for Stroke to Europe with CE Mark for THUNDERBOLT - BioSpace
Penumbra Expands CAVT for Stroke to Europe with CE Mark for THUNDERBOLT BioSpace
Penumbra’s FDA nod for clot removal tech a win for Boston Scientific - MedTech Dive
Penumbra’s FDA nod for clot removal tech a win for Boston Scientific MedTech Dive
Showing 6 of 10 news items
Based on last 4 crawl cycles
Source: USCIS H-1B Employer Data Hub
Recent peer-reviewed publications with author affiliations at this company
Developing a Coordinated Registry Network for devices used for acute ischemic stroke intervention: basilar artery occlusion quality assessment pilot.
Standardized approach to direct first pass aspiration technique for endovascular thrombectomy: Description and initial experience with CANADAPT.
Showing 5 of 10 publications
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