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Elevator, Ent

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

1,159
Registered devices
21
Adverse events
1
Recalls
5
510(k) clearances

Devices with this code

PILLING — TELEFLEX INCORPORATEDVan Sickle — VAN SICKLE SURGICAL INSTRUMENTS, INCORPORATEDAmbler Surgical — AMBLER SURGICAL CORP.Ambler Surgical — AMBLER SURGICAL CORP.RZ Medizintechnik GmbH — RZ-Medizintechnik GmbHCRONIN CLEFT PALATE ELEVATOR — SONTEC INSTRUMENTS, INC.Integra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONBEAR — Bear-Ent, LLCAmbler Surgical — AMBLER SURGICAL CORP.Instrumentarium — Société Chirurgicale Instrumentarium IncNovo Surgical Inc. — NOVO SURGICAL, INC.RZ Medizintechnik GmbH — RZ-Medizintechnik GmbHBOSS Instruments — BOSS INSTRUMENTS, LTD., INC.Quinelato — Schobell Industrial LtdaSklar® — SKLAR CORPORATIONAmbler Surgical — AMBLER SURGICAL CORP.PILLING — TELEFLEX INCORPORATEDV. Mueller — STERIS CORPORATIONAvalign — Avalign Technologies, Inc.Bausch + Lomb — Bausch & Lomb IncorporatedgSource — GSOURCE LLCSklar® — SKLAR CORPORATIONHELMUT ZEPF — Helmut Zepf Medizintechnik GmbH

Recent recalls

DateFirmReason
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.

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