Home › Device types › LZJ
Prosthesis, Toe (Metatarsophalangeal), Joint, Metal/Polymer, Semi-Constrained
FDA product code LZJ · Class U · Unknown
134
Registered devices
79
Adverse events
1
Recalls
11
510(k) clearances
Devices with this code
HemiCAP® — ARTHROSURFACE INCORPORATEDOsteoMed — OSTEOMED LLCOsteoMed — OSTEOMED LLCOsteoMed — OSTEOMED LLCOsteoMed — OSTEOMED LLCToeMobile™ Phalangeal Implant — Merete GmbHOsteoMed — OSTEOMED LLCTOTAL TOE SYSTEM — Biomet Orthopedics, LLCOsteoMed — OSTEOMED LLCOsteoMed — OSTEOMED LLCOsteoMed — OSTEOMED LLCMovement Great Toe System — Smith & Nephew, Inc.OsteoMed — OSTEOMED LLCOsteoMed — OSTEOMED LLCMovement Great Toe System — Smith & Nephew, Inc.OsteoMed — OSTEOMED LLCMovement Great Toe System — Smith & Nephew, Inc.OsteoMed — OSTEOMED LLCOsteoMed — OSTEOMED LLCKGTI™ Kinetik Great Toe Implant System — Ascension Orthopedics, Inc.OsteoMed — OSTEOMED LLCToe MotionTM — ARTHROSURFACE INCORPORATEDOsteoMed — OSTEOMED LLCOsteoMed — OSTEOMED LLC
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2014-06-09 | Arthrosurface, Inc. | An oversight in the implementation of the design change record resulted in outdated components being shipped to customers. The component did not pass a half-cyc |
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