Home › Device types › JDL
Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)
FDA product code JDL · Class 3 · Orthopedic
575
Registered devices
3,888
Adverse events
5
Recalls
45
510(k) clearances
Devices with this code
Duracon — Howmedica Osteonics Corp.CONSERVE® — Microport Orthopedics Inc.CLS® Brevius® Kinectiv® — Zimmer GmbHTRANSCEND® — Microport Orthopedics Inc.Compress Device — Biomet Orthopedics, LLCCONSERVE® — Microport Orthopedics Inc.Consensus Hip System — Shalby Advanced Technologies, Inc.CONSERVE® — Microport Orthopedics Inc.Compress® Device — Biomet Orthopedics, LLCConsensus Hip System — Shalby Advanced Technologies, Inc.Compress® Device — Biomet Orthopedics, LLCFitmore® Hip Stem — Zimmer GmbHOmnifit — Howmedica Osteonics Corp.Dynasty — Microport Orthopedics Inc.CLS® Brevius® Kinectiv® — Zimmer GmbHOmnifit — Howmedica Osteonics Corp.Fitmore® Hip Stem — Zimmer GmbHTaperloc Complete Micro Primary Femoral — Biomet Orthopedics, LLCDuracon — Howmedica Osteonics Corp.Consensus® Hip System — CONSENSUS ORTHOPEDICS, INC.Consensus Hip System — Shalby Advanced Technologies, Inc.Omnifit — Howmedica Osteonics Corp.Consensus® Hip System — CONSENSUS ORTHOPEDICS, INC.CONSERVE® — Microport Orthopedics Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-07-30 | Howmedica Osteonics Corp. | Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential f |
| 2010-06-07 | Wright Medical Technology Inc | The inner and outer product packaging was missing the following information: shelf life, translations, manufacturing date, CE marking and also listed the incor |
| 2009-05-14 | Wright Medical Technology Inc | Incorrect packaging, swapped sizes |
| 2009-05-14 | Wright Medical Technology Inc | Incorrect packaging, swapped sizes |
| 2004-01-09 | Stryker Howmedica Osteonics | This device is not approved for sale in the US. |
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