Home › Device types › KOX
Solvent, Adhesive Tape
FDA product code KOX · Class 1 · General, Plastic Surgery
126
Registered devices
81
Adverse events
3
Recalls
12
510(k) clearances
Devices with this code
ALLKARE — CONVATEC, PURCHASING DEPARTMENTGluGone Adhesive Remover, 2 oz. — Chemence Medical, Inc.LP — La Pointique International, Ltd.Micro-Scientific Goo Gone Topical and Surface Adhesive Remover — MICRO-SCIENTIFIC, LLCMaxtaping A+ — La Pointique International, Ltd.OSSEOUS- Adhesion Remover Pad — EON MEDITECH PRIVATE LIMITEDMaxtaping A+ — Oppo Medical Inc.REMOVE Adhesive Remover 8oz US — SMITH & NEPHEW MEDICAL LIMITEDMaxtaping A+ — Oppo Medical Inc.Maxtaping — Oppo Medical Inc.Uni-Patch — Cardinal Health, Inc.Maxtaping A+ — La Pointique International, Ltd.Maxtaping A+ — Oppo Medical Inc.Maxtaping — La Pointique International, Ltd.REMOVE Wipes — SMITH & NEPHEW MEDICAL LIMITEDDETACHOL — FERNDALE LABORATORIES, INC.Maxtaping — Oppo Medical Inc.Maxtaping A+ — Oppo Medical Inc.FreeDerm — ARGENTUM MEDICAL, LLCMaxtaping A+ — Oppo Medical Inc.Maxtaping — La Pointique International, Ltd.Brava — Coloplast A/SLP — La Pointique International, Ltd.Kendall — Cardinal Health, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2011-04-04 | Smith & Nephew Inc. | Smith & Nephew, Inc., St. Petersburg, FL is recalling multiple lot numbers of the following products: REMOVE Universal Adhesive Remover Wipes, UNI-SOLVE Adhesi |
| 2011-04-04 | Smith & Nephew Inc. | Smith & Nephew, Inc., St. Petersburg, FL is recalling multiple lot numbers of the following products: REMOVE Universal Adhesive Remover Wipes, UNI-SOLVE Adhesi |
| 2010-07-07 | Ferndale Laboratories, Inc. | There is a defect on the neck surface of the bottles, causing bottles to leak. Bottle defect may potentially cause contamination of solvent stored in bottles. |
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