Home › Device types › GBA
Catheter, Balloon Type
FDA product code GBA · Class 1 · General, Plastic Surgery
13
Registered devices
751
Adverse events
1
Recalls
5
510(k) clearances
Devices with this code
Verify — SPINEOLOGY INC.CooperSurgical, Inc. — Coopersurgical, Inc.GOBEN — HUZHOU JUNDA INDUSTRY CO., LTD.n.a. — Karl Storz GmbH & Co. KGn.a. — Karl Storz GmbH & Co. KGPneumatic Inflator — BOSTON SCIENTIFIC CORPORATIONn.a. — Karl Storz GmbH & Co. KGCustom Medical Specialties, Inc. — CUSTOM ASSEMBLIES, INC.Symmetry Surgical® — ASPEN SURGICAL PRODUCTS, INC.n.a. — Karl Storz GmbH & Co. KGn.a. — Karl Storz GmbH & Co. KGn.a. — Karl Storz GmbH & Co. KGRUSCH — TELEFLEX INCORPORATED
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-05-31 | Karl Storz Endoscopy America Inc | Karl Storz Endoscopy-America has initiated the recall of the 27023WU Balloon Catheter because the packaging may be compromised, and therefore the sterility of t |
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