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Medicon

Medicon eG. Chirurgiemechaniker-Genossenschaft · Model 51.79.02 · UDI-DI 04046826063023

EZO Prescription
5
510(k) clearances
69
Adverse events
1
Recalls
37
Facilities

Description

Otis urethrotome complete

Recalls

DateFirmReason
2010-12-22Olympus America Inc.The device sterile package seal shows evidence of being breached or was breached

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.