Home › Device types › KAK
Probe, Ent
FDA product code KAK · Class 1 · Ear, Nose, Throat
373
Registered devices
7
Adverse events
1
Recalls
1
510(k) clearances
Devices with this code
BEAR — Bear-Ent, LLCFENTEX — FENTEX medical GmbHSymmetry Jako — ASPEN SURGICAL PRODUCTS, INC.Salivary duct probe — Spiggle & Theis Medizintechnik GmbHFENTEX — FENTEX medical GmbHPILLING — TELEFLEX INCORPORATEDMicroFrance® — INTEGRA MICROFRANCEMSI Precision Specialty Instruments — Med Saver, Inc.Integra® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONMicroFrance® — INTEGRA MICROFRANCEFENTEX — FENTEX medical GmbHFENTEX — FENTEX medical GmbHProbe — KOROS U.S.A., INC.Novo Surgical — NOVO SURGICAL, INC.FENTEX — FENTEX medical GmbHBowman salivary duct probe — Spiggle & Theis Medizintechnik GmbHMSI Precision Specialty Instruments — Med Saver, Inc.MicroFrance® — INTEGRA MICROFRANCESalivary duct probe — Spiggle & Theis Medizintechnik GmbHMicroFrance® — INTEGRA MICROFRANCENA — Richard Wolf GmbHBall Probe — KOROS U.S.A., INC.Millennium — Avalign Technologies, Inc.V. Mueller — STERIS CORPORATION
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2012-08-17 | Vital Signs Colorado Inc. | There is a potential for epistaxis during use of the Disposable General Purpose 9 French Temperature Probe. |
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.