Home › Device types › MBH
Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
FDA product code MBH · Class 2 · Orthopedic
28,849
Registered devices
16,331
Adverse events
102
Recalls
143
510(k) clearances
Devices with this code
INSTRUMENT — Howmedica Osteonics Corp.PROPHECY — Microport Orthopedics Inc.Truliant — Exactech, Inc.AGC V2 TOTAL KNEE SYSTEM — Biomet Orthopedics, LLCVanguard® SSK Knee System — Biomet Orthopedics, LLCVANGUARD 360 — Biomet Orthopedics, LLCVanguard Knee System — Biomet Orthopedics, LLCPERSONA™ Trabecular Metal™ — Zimmer, Inc.Evolution — Microport Orthopedics Inc.Prophecy — Microport Orthopedics Inc.Prophecy — Microport Orthopedics Inc.Prophecy — Microport Orthopedics Inc.NA — Exactech, Inc.VANGUARD 360 — Biomet Orthopedics, LLCVanguard® — Biomet Orthopedics, LLCPointCloud Knee Instruments — Unik Orthopedics Inc.Vanguard® Complete Knee System — Biomet Orthopedics, LLCVanguard® Complete Knee System — Biomet Orthopedics, LLCU2 Total Knee System — UNITED ORTHOPEDIC CORP.Persona® The Personalized Knee® System — Zimmer, Inc.PROPHECY — Microport Orthopedics Inc.PROPHECY — Microport Orthopedics Inc.PROPHECY — Microport Orthopedics Inc.Prophecy — Microport Orthopedics Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-05-19 | Howmedica Osteonics Corp. | Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TY |
| 2026-05-19 | Howmedica Osteonics Corp. | Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TY |
| 2026-05-11 | Zimmer, Inc. | Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package. |
| 2024-10-29 | MicroPort Orthopedics Inc. | Femoral implant porous size 5 right primary and femoral implant non-porous size 6 left primary have correct markings on devices, but may have incorrect packagin |
| 2024-03-13 | Biomet, Inc. | Possible damage to the Vanguard Knee System AS Tibial Bearing caused during the manufacturing process. |
| 2024-03-12 | DePuy Orthopaedics, Inc. | Product incorrectly labelled. |
| 2024-02-06 | Howmedica Osteonics Corp. | Potential packaging breaches of inner blister and outer sterile blister. |
| 2024-02-06 | Howmedica Osteonics Corp. | Potential packaging breaches of inner blister and outer sterile blister. |
| 2024-02-06 | Howmedica Osteonics Corp. | Potential packaging breaches of inner blister and outer sterile blister. |
| 2024-02-06 | Howmedica Osteonics Corp. | Potential packaging breaches of inner blister and outer sterile blister. |
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