Home › Device types › KCB
Tube, Tonsil Suction
FDA product code KCB · Class 1 · Ear, Nose, Throat
979
Registered devices
8
Adverse events
1
Recalls
1
510(k) clearances
Devices with this code
HNM MEDICAL — HNM STAINLESS, LLC.SUCTION TUBE — KLS-Martin L.P.Novo Surgical Inc. — NOVO SURGICAL, INC.Surgical Direct — Surgical Direct, Inc.SUCTION TUBE — KLS-Martin L.P.Novo Surgical Inc. — NOVO SURGICAL, INC.MicroFrance® — INTEGRA MICROFRANCEmytaMed — Mytamed, Inc.SUCTION TUBE — KLS-Martin L.P.Surgical Direct — Surgical Direct, Inc.mytaMed — Mytamed, Inc.V. Mueller — STERIS CORPORATIONSurgical Direct — Surgical Direct, Inc.SUCTION TUBE — KLS-Martin L.P.Surgical Direct — Surgical Direct, Inc.Surgical Direct — Surgical Direct, Inc.Novo Surgical Inc. — NOVO SURGICAL, INC.Surgical Direct — Surgical Direct, Inc.Novo Surgical — NOVO SURGICAL, INC.Surgical Direct — Surgical Direct, Inc.Surgical Direct — Surgical Direct, Inc.devemed — devemed GmbHMicroFrance® — INTEGRA MICROFRANCENovo Surgical Inc. — NOVO SURGICAL, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-04-08 | MEDLINE INDUSTRIES, LP - Northfield | Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have bee |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.