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Curette, Adenoid

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

361
Registered devices
2
Adverse events
1
Recalls
1
510(k) clearances

Devices with this code

Gimmi — Gimmi GmbHSklar — SKLAR CORPORATIONHayden Medical — Hayden Medical, Inc.MSI Precision Specialty Instruments — Med Saver, Inc.Quinelato — Schobell Industrial LtdaNovo Surgical Inc. — NOVO SURGICAL, INC.Integra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONIntegra® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONMedicon — Medicon eG. Chirurgiemechaniker-GenossenschaftNovo Surgical — NOVO SURGICAL, INC.Ambler Surgical — AMBLER SURGICAL CORP.Novo Surgical — NOVO SURGICAL, INC.BARNHILL ADENOID CURETTE — SONTEC INSTRUMENTS, INC.Integra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONV. Mueller — STERIS CORPORATIONPILLING — TELEFLEX INCORPORATEDPILLING — TELEFLEX INCORPORATEDIntegra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONMSI Precision Specialty Instruments — Med Saver, Inc.MSI Precision Specialty Instruments — Med Saver, Inc.MILLENNIUM — Avalign Technologies, Inc.V. Mueller — STERIS CORPORATIONAESCULAP — Aesculap AGSklar — SKLAR CORPORATION

Recent recalls

DateFirmReason
2004-01-29Medtronic Xomed, Inc.The box label indicates that the product is a size 2 whereas a size 4 was packed inside.

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