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
Profix — Smith & Nephew, Inc.Sgarlato Silastic — FUSION ORTHOPEDICS, LLCPROFIX — Smith & Nephew, Inc.Silicone Toe System — Smith & Nephew, Inc.PROFIX — Smith & Nephew, Inc.SWANSON — WRIGHT MEDICAL TECHNOLOGY, INC.ORTHOFLEX — WRIGHT MEDICAL TECHNOLOGY, INC.Profix — Smith & Nephew, Inc.ORTHOFLEX — WRIGHT MEDICAL TECHNOLOGY, INC.SWANSON — WRIGHT MEDICAL TECHNOLOGY, INC.PROFIX — Smith & Nephew, Inc.OsteoMed — OSTEOMED LLCTaperloc Complete Micro Primary Femoral — Biomet Orthopedics, LLCTaperloc Complete Micro Primary Femoral — Biomet Orthopedics, LLCTaperloc Complete Micro Primary Femoral — Biomet Orthopedics, LLCPROFIX — Smith & Nephew, Inc.Taperloc Complete Micro Primary Femoral — Biomet Orthopedics, LLCProfix — Smith & Nephew, Inc.Sgarlato Silastic — FUSION ORTHOPEDICS, LLCPROFIX — Smith & Nephew, Inc.ASCENT KNEE SYSTEM — Biomet Orthopedics, LLCPROFIX — Smith & Nephew, Inc.SWANSON — WRIGHT MEDICAL TECHNOLOGY, INC.ASCENT KNEE SYSTEM — Biomet Orthopedics, LLC
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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