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Forceps, Ent

FDA product code KAE · Class 1 · Ear, Nose, Throat

5,473
Registered devices
82
Adverse events
1
Recalls
14
510(k) clearances

Devices with this code

NA — Richard Wolf GmbHAmbler Surgical — AMBLER SURGICAL CORP.Ambler Surgical — AMBLER SURGICAL CORP.HNM MEDICAL — HNM STAINLESS, LLC.Hayden Medical — Hayden Medical, Inc.Blakesley nasal forceps, Black Line — Spiggle & Theis Medizintechnik GmbHBR Surgical, LLC — BR Surgical, LLCRZ Medizintechnik GmbH — RZ-Medizintechnik GmbHAESCULAP — AESCULAP, INC.Medicon — Medicon eG. Chirurgiemechaniker-GenossenschaftIntegra® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONIntegra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONGruenwald Bayonet Forceps — SONTEC INSTRUMENTS, INC.JEDMED — JEDMED INSTRUMENT COMPANYNovo Surgical Inc. — NOVO SURGICAL, INC.MILLENNIUM — Avalign Technologies, Inc.PILLING — TELEFLEX INCORPORATEDBR Surgical, LLC — BR Surgical, LLCRZ Medizintechnik GmbH — RZ-Medizintechnik GmbHIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONHNM MEDICAL — HNM STAINLESS, LLC.Symmetry Blake — ASPEN SURGICAL PRODUCTS, INC.BR Surgical, LLC — BR Surgical, LLCV. Mueller — STERIS CORPORATION

Recent recalls

DateFirmReason
2025-01-31Aesculap IncThe forceps have been used in ways not covered by the design resulting in breakage of the clamps.

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