Home › Device types › KDH
Catheter (Gastric, Colonic, Etc.), Irrigation And Aspiration
FDA product code KDH · Class 2 · Gastroenterology, Urology
45
Registered devices
66
Adverse events
2
Recalls
23
510(k) clearances
Devices with this code
Axiom® — AXIOM MEDICAL, INCORPORATEDAxiom® — AXIOM MEDICAL, INCORPORATEDAspiration Tubing — ARMM INC.Silber — COOK INCORPORATEDHalyard — Avanos Medical, Inc.Axiom® — AXIOM MEDICAL, INCORPORATEDEthox Medical — ETHOX MEDICAL, LLCArgyle — Cardinal Health, Inc.Halyard — Avanos Medical, Inc.Ethox Medical — ETHOX MEDICAL, LLCSuperFlow Tubing Set — ARMM INC.Argyle — Cardinal Health 200, LLCAxiom® — AXIOM MEDICAL, INCORPORATEDInjection Needle Catheter — Avanos Medical, Inc.Axiom® — AXIOM MEDICAL, INCORPORATEDAxiom® — AXIOM MEDICAL, INCORPORATEDEthox Medical — ETHOX MEDICAL, LLCEthox Medical — ETHOX MEDICAL, LLCAxiom® — AXIOM MEDICAL, INCORPORATEDSuperFlow Tubing Set — ARMM INC.Axiom® — AXIOM MEDICAL, INCORPORATEDEthox Medical — ETHOX MEDICAL, LLCAspiration Tubing — ARMM INC.Curaplex — BOUND TREE MEDICAL, LLC
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-02-23 | MEDLINE INDUSTRIES, LP - Northfield | Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users. |
| 2012-05-10 | MEDDEV USA, INC. | The device was marketed without a 510(k) and is not sterile. |
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