Home › Device types › LPH
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
FDA product code LPH · Class 2 · Orthopedic
34,506
Registered devices
89,776
Adverse events
297
Recalls
563
510(k) clearances
Devices with this code
Logical Face Changing Liner — SIGNATURE ORTHOPAEDICS PTY LTDSpartan Hip Stem — SIGNATURE ORTHOPAEDICS PTY LTDDELTA LINERS & ACCESSORIES — LIMACORPORATE SPAEcho® Bi-Metric® Microplasty® Hip Stem — Biomet Orthopedics, LLCIconacy i-Hip — Iconacy Orthopedic Implants LLCPantheon System — ADLER ORTHO SPASUMMIT POROCOAT — DEPUY ORTHOPAEDICS, INC.U2™ Hip — UNITED ORTHOPEDIC CORP.Secur-Fit — Howmedica Osteonics Corp.USTAR II Knee System — UNITED ORTHOPEDIC CORP.Trident — Howmedica Osteonics Corp.V40 Head — Howmedica Osteonics Corp.Accolade — Howmedica Osteonics Corp.BENCOX Hip System — Corentec Co., LtdMINIMA S — LIMACORPORATE SPADELTA LINERS & ACCESSORIES — LIMACORPORATE SPAWorld Cup Trial Liner - 32B Hooded 10° — SIGNATURE ORTHOPAEDICS PTY LTDMobileLink Acetabular Cup System — WALDEMAR LINK GmbH & Co. KGTRIDENT II — Howmedica Osteonics Corp.Origin DAA Stem, Standard Offset — SIGNATURE ORTHOPAEDICS PTY LTDOrigin Hip Stem — SIGNATURE ORTHOPAEDICS PTY LTDWorld Hip Stem Size 2M — SIGNATURE ORTHOPAEDICS PTY LTDINSTRUMENT — Howmedica Osteonics Corp.INSTRUMENT — Howmedica Osteonics Corp.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-01-05 | Encore Medical, LP | 942-01-40G acetabular system package was found to contain 942-01-36H acetabular system; and several other acetabular system and knee insert devices may also hav |
| 2025-09-26 | Zimmer, Inc. | Zimmer Biomet is conducting a medical device recall for two (2) lots of the Dual Mobility Vivacit-E Bearing due to a commingle. The outer package is labeled as |
| 2025-09-26 | Zimmer, Inc. | Zimmer Biomet is conducting a medical device recall for two (2) lots of the Dual Mobility Vivacit-E Bearing due to a commingle. The outer package is labeled as |
| 2025-09-09 | BioPro, Inc. | Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infectio |
| 2025-09-09 | BioPro, Inc. | Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infectio |
| 2025-06-12 | Encore Medical, LP | Due to packaging discrepancy with the incorrect tibial inserts/implants being packaged. Issued discovered via a customer complaint. |
| 2025-06-12 | Encore Medical, LP | Due to packaging discrepancy with the incorrect tibial inserts/implants being packaged. Issued discovered via a customer complaint. |
| 2025-03-25 | Conformis Inc. | The hip cup liner that was packaged with the incorrect labeling. HDL-060-C22S-000101 from Lot 1788258 contained a hooded liner, but it was labeled to have a sta |
| 2024-12-31 | Exactech, Inc. | Due to the lack of the Ethylene Vinyl Alcohol (EVOH) barrier layer. |
| 2024-09-19 | Novosource, LLC | Mislabeled: Packaged in a box labeled as 32 long but containing a 28 long head by physical marking, may result in joint instability if implanted |
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