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Trephine, Manual, Ophthalmic

FDA product code HRH · Class 1 · Ophthalmic

1,019

Registered devices

23

Adverse events

1

Recalls

12

510(k) clearances

Devices with this code

N.A. — Geuder Aktiengesellschaft coronet — NETWORK MEDICAL PRODUCTS LIMITED Coronet — NETWORK MEDICAL PRODUCTS LIMITED Corneal Trephine — KATENA PRODUCTS, INC.SURGISTAR, INC. — SURGISTAR, INC.Bausch + Lomb — Bausch & Lomb Incorporated SURGISTAR — SURGISTAR, INC.Coronet — NETWORK MEDICAL PRODUCTS LIMITED Bausch + Lomb — Bausch & Lomb Incorporated SURGISTAR — SURGISTAR, INC.Coronet — CorneaGen LLC Coronet — NETWORK MEDICAL PRODUCTS LIMITED CORNEAL TREPHINE HANDLE 7.5MM — KATENA PRODUCTS, INC.coronet — NETWORK MEDICAL PRODUCTS LIMITED Ambler Surgical — AMBLER SURGICAL CORP.Bausch + Lomb — Bausch & Lomb Incorporated SURGISTAR — SURGISTAR, INC.Coronet — NETWORK MEDICAL PRODUCTS LIMITED CORNEAL TREPHINE BLADE 6.7MM — KATENA PRODUCTS, INC.SURGISTAR — SURGISTAR, INC.SURGISTAR — SURGISTAR, INC.CORNEAL TREPHINE BLADE 7.7MM — KATENA PRODUCTS, INC.CORNEAL TREPHINE DEPTH GAUGE — SONTEC INSTRUMENTS, INC.Millennium — Avalign Technologies, Inc.

Recent recalls

Date	Firm	Reason
2013-05-03	Surgical Instrument Service And Savings, Inc.	The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.