Home › Device types › KCG
Dilator, Tracheal
FDA product code KCG · Class 1 · Ear, Nose, Throat
82
Registered devices
21
Adverse events
1
Recalls
1
510(k) clearances
Devices with this code
PILLING — TELEFLEX INCORPORATEDSymmetry Laborde — ASPEN SURGICAL PRODUCTS, INC.PILLING — TELEFLEX INCORPORATEDNovo Surgical Inc. — NOVO SURGICAL, INC.V. Mueller — STERIS CORPORATIONIntegra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONPILLING — TELEFLEX INCORPORATEDSymmetry Laborde — ASPEN SURGICAL PRODUCTS, INC.InHealth Technologies; Blom-Singer — Freudenberg Medical, LLCPILLING — TELEFLEX INCORPORATEDMedicon — Medicon eG. Chirurgiemechaniker-GenossenschaftSymmetry Trousseau — ASPEN SURGICAL PRODUCTS, INC.DILATOR — KLS-Martin L.P.BR Surgical, LLC — BR Surgical, LLCPILLING — TELEFLEX INCORPORATEDPILLING — TELEFLEX INCORPORATEDPILLING — TELEFLEX INCORPORATEDGimmi — Gimmi GmbHPILLING — TELEFLEX INCORPORATEDInHealth Technologies; Blom-Singer — Freudenberg Medical, LLCIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONSklar — SKLAR CORPORATIONLaborde Dilator Forcep — N S SURGICAL COMPANYPILLING — TELEFLEX INCORPORATED
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-12-03 | Sklar Instruments | Reports of various packaging issues that may result in a breach of the sterile barrier. |
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.