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Tube, Tonsil Suction

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

983
Registered devices
9
Adverse events
1
Recalls
1
510(k) clearances

Devices with this code

MicroFrance® — INTEGRA MICROFRANCEHNM MEDICAL — HNM STAINLESS, LLC.TUBE — KLS-Martin L.P.Surgical Direct — Surgical Direct, Inc.Surgical Direct — Surgical Direct, Inc.mytaMed — Mytamed, Inc.Surgical Direct — Surgical Direct, Inc.Surgical Direct — Surgical Direct, Inc.Surgical Direct — Surgical Direct, Inc.SUCTION TUBE — KLS-Martin L.P.Novo Surgical Inc. — NOVO SURGICAL, INC.devemed — devemed GmbHNovo Surgical Inc. — NOVO SURGICAL, INC.Millennium — Avalign Technologies, Inc.MicroFrance® — INTEGRA MICROFRANCEMillennium — Avalign Technologies, Inc.Surgical Direct — Surgical Direct, Inc.SUCTION TUBE — KLS-Martin L.P.Surgical Direct — Surgical Direct, Inc.Millennium — Avalign Technologies, Inc.Medicon — Medicon eG. Chirurgiemechaniker-GenossenschaftMillennium — Avalign Technologies, Inc.PILLING — TELEFLEX INCORPORATEDSurgical Direct — Surgical Direct, Inc.

Recent recalls

DateFirmReason
2024-04-08MEDLINE INDUSTRIES, LP - NorthfieldMedical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have bee

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