Home › Device types › KWH
Prosthesis, Toe, Constrained, Polymer
FDA product code KWH · Class 2 · Orthopedic
341
Registered devices
149
Adverse events
2
Recalls
21
510(k) clearances
Devices with this code
OsteoMed — OSTEOMED LLCSWANSON — WRIGHT MEDICAL TECHNOLOGY, INC.Profix — Smith & Nephew, Inc.PROFIX — Smith & Nephew, Inc.PROFIX — Smith & Nephew, Inc.PROFIX — Smith & Nephew, Inc.PROFIX — Smith & Nephew, Inc.Futura™ FGT — TORNIER, INC.Integra® — Ascension Orthopedics, Inc.PROFIX — Smith & Nephew, Inc.PROFIX — Smith & Nephew, Inc.PROFIX — Smith & Nephew, Inc.Sgarlato Silastic — FUSION ORTHOPEDICS, LLCPROFIX — Smith & Nephew, Inc.Profix — Smith & Nephew, Inc.Sgarlato Silastic — FUSION ORTHOPEDICS, LLCPROFIX — Smith & Nephew, Inc.Taperloc Complete Micro Primary Femoral — Biomet Orthopedics, LLCTaperloc Complete Micro Primary Femoral — Biomet Orthopedics, LLCRTS — In2Bones USA, LLCSgarlato Silastic — FUSION ORTHOPEDICS, LLCSWANSON — WRIGHT MEDICAL TECHNOLOGY, INC.Sgarlato Silastic — FUSION ORTHOPEDICS, LLCFutura™ CGT — TORNIER, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2009-04-06 | Tornier, Inc. | Tornier, Inc. has received a report of a mislabeled product due to a product mix-up. The package label indicated that the product was a model LMP-50 however th |
| 2009-03-01 | Sgarlato Med, LLC | Products with an expiration date of August, 2009 were labeled with an expiration date of May 2013. Additionally, the outer packages were labeled with an incorre |
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