Home › Device types › KFX
Assembly, Thigh/Knee/Shank/Ankle/Foot, External
FDA product code KFX · Class 2 · Physical Medicine
13
Registered devices
3
Adverse events
3
Recalls
4
510(k) clearances
Devices with this code
MIRABRUSH YELLOW POINTED — HAGER WORLDWIDE, INC.VascuTape Radiopaque Tape — Lemaitre Vascular, Inc.YES Tape — Lemaitre Vascular, Inc.Vesper Custom Tape — Lemaitre Vascular, Inc.VascuTape Radiopaque Tape — Lemaitre Vascular, Inc.VascuTape Radiopaque Tape — Lemaitre Vascular, Inc.VascuTape Radiopaque Tape — Lemaitre Vascular, Inc.VascuTape Radiopaque Tape — Lemaitre Vascular, Inc.VascuTape Radiopaque Tape — Lemaitre Vascular, Inc.MIRABRUSH BLUE STRAIGHT — HAGER WORLDWIDE, INC.VascuTape Radiopaque Tape — Lemaitre Vascular, Inc.VascuTape Radiopaque Tape — Lemaitre Vascular, Inc.VascuTape Radiopaque Tape — Lemaitre Vascular, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-03-18 | LeMaitre Vascular, Inc. | Devices were not sealed correctly during the manufacturing process, and the sterility of these products have been compromised. |
| 2013-03-18 | LeMaitre Vascular, Inc. | Devices were not sealed correctly during the manufacturing process, and the sterility of these products have been compromised. |
| 2006-08-10 | Bock,Otto,Orthopedic Ind,Inc | A correction of the Otto Bock Compact prosthetic knee joint, material numbers 3C93 and 3C85, is being conducted. A limited number of Compacts have a defective |
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