Home › Device types › EZO
Urethrotome
FDA product code EZO · Class 2 · Gastroenterology, Urology
213
Registered devices
69
Adverse events
1
Recalls
5
510(k) clearances
Devices with this code
Olympus — OLYMPUS Winter & Ibe GmbHAED — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.AED — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.n.a. — Karl Storz GmbH & Co. KGAED — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.E-LINE — Richard Wolf GmbHn.a. — Karl Storz GmbH & Co. KGAED — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.Greenwald Surgical Company, Inc. — GRACE MANUFACTURING, INC.Urethrotomy sheath — SOPRO-COMEG GmbHAED — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.AED — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.NA — Richard Wolf GmbHUrethrotomy sheath — SOPRO-COMEG GmbHAED — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.Urethrotomy knife — SOPRO-COMEG GmbHAED — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.Olympus — OLYMPUS Winter & Ibe GmbHAED — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.Novo Surgical — NOVO SURGICAL, INC.V. Mueller — STERIS CORPORATIONAED — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.AED — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.AED — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-12-22 | Olympus America Inc. | The device sterile package seal shows evidence of being breached or was breached |
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