Home › Device types › KCL
Blower, Powder, Ent
FDA product code KCL · Class 1 · Ear, Nose, Throat
23
Registered devices
2
Adverse events
0
Recalls
0
510(k) clearances
Devices with this code
n.a. — Karl Storz GmbH & Co. KGDryswab — MEDICAL WIRE & EQUIPMENT CO.(BATH)LIMITEDn.a. — Karl Storz GmbH & Co. KGn.a. — Karl Storz GmbH & Co. KGSHEEHY-HOUSE POWDER INSUFFLATOR — Oto-Med, Inc.n.a. — Karl Storz GmbH & Co. KGn.a. — Karl Storz GmbH & Co. KGn.a. — Karl Storz GmbH & Co. KGn.a. — Karl Storz GmbH & Co. KGn.a. — Karl Storz GmbH & Co. KGKABIERSKE POWDER BLOWER CANNULA — SONTEC INSTRUMENTS, INC.n.a. — Karl Storz GmbH & Co. KGn.a. — Karl Storz GmbH & Co. KGn.a. — Karl Storz GmbH & Co. KGKABIERSKE POWDER BLOWER SET — SONTEC INSTRUMENTS, INC.BR Surgical, LLC — BR Surgical, LLCBR Surgical, LLC — BR Surgical, LLCn.a. — Karl Storz GmbH & Co. KGn.a. — Karl Storz GmbH & Co. KGBR Surgical, LLC — BR Surgical, LLCn.a. — Karl Storz GmbH & Co. KGn.a. — Karl Storz GmbH & Co. KGn.a. — Karl Storz GmbH & Co. KG
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.