Home › Device types › GBA
Catheter, Balloon Type
FDA product code GBA · Class 1 · General, Plastic Surgery
15
Registered devices
756
Adverse events
1
Recalls
5
510(k) clearances
Devices with this code
n.a. — Karl Storz GmbH & Co. KGCooperSurgical, Inc. — Coopersurgical, Inc.GOBEN — HUZHOU JUNDA INDUSTRY CO., LTD.Envision — SPINAL STABILIZATION TECHNOLOGIES LIMITEDn.a. — Karl Storz GmbH & Co. KGEnvision — SPINAL STABILIZATION TECHNOLOGIES LIMITEDn.a. — Karl Storz GmbH & Co. KGn.a. — Karl Storz GmbH & Co. KGPneumatic Inflator — BOSTON SCIENTIFIC CORPORATIONSymmetry Surgical® — ASPEN SURGICAL PRODUCTS, INC.n.a. — Karl Storz GmbH & Co. KGn.a. — Karl Storz GmbH & Co. KGRUSCH — TELEFLEX INCORPORATEDVerify — SPINEOLOGY INC.Custom Medical Specialties, Inc. — CUSTOM ASSEMBLIES, INC.
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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