Home › Device types › LZO
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
FDA product code LZO · Class 2 · Orthopedic
32,067
Registered devices
33,109
Adverse events
177
Recalls
535
510(k) clearances
Devices with this code
InSitu Hip System — NEXTSTEP ARTHROPEDIX, LLCTAPERLOC COMPLETE RASP/PROVISIONAL — Biomet Orthopedics, LLCArcos Modular Revision Hip System — Biomet Orthopedics, LLCEcho® Press-Fit Hip System — Biomet Orthopedics, LLCUSTAR II Knee System — UNITED ORTHOPEDIC CORP.iTotal® Hip Replacement System — Conformis, Inc.PROFEMUR® — Microport Orthopedics Inc.Libertas — MAXX ORTHOPEDICS, INC.Libertas — MAXX ORTHOPEDICS, INC.SP-CL Hip Stem — WALDEMAR LINK GmbH & Co. KGArcos® Revision Hip Instrumentation — Biomet Uk LtdUnited Hip System — UNITED ORTHOPEDIC CORP.Trident — Howmedica Osteonics Corp.OSS™ Orthopedic Salvage System — Biomet Orthopedics, LLCPINNACLE GRIPTION — DEPUY ORTHOPAEDICS, INC.Continuum® Trabecular Metal™ — Zimmer, Inc.Kyocera Medical Technologies, Inc. — KYOCERA MEDICAL TECHNOLOGIES, INC.Endo-Model SL Knee Prosthesis System — WALDEMAR LINK GmbH & Co. KGINSTRUMENT — Howmedica Osteonics Corp.Continuum® Trilogy® Allofit® Longevity® — Zimmer, Inc.NA — Zimmer, Inc.RINGLOC RX90-2 HIP SYSTEM — Biomet Orthopedics, LLCCorin TriFit CF Hip Stem — CORIN LTDMiniHip Stem — CORIN LTD
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 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 |
| 2025-03-24 | Zimmer, Inc. | The associated product labeling does not adequately provide compatibility information for use of the 22.2 mm Diameter Ceramic Femoral Heads with cobalt-chrome f |
| 2025-03-24 | Zimmer, Inc. | The associated product labeling does not adequately provide compatibility information for use of the 22.2 mm Diameter Ceramic Femoral Heads with cobalt-chrome f |
| 2025-03-24 | Zimmer, Inc. | The associated product labeling does not adequately provide compatibility information for use of the 22.2 mm Diameter Ceramic Femoral Heads with cobalt-chrome f |
| 2025-03-24 | Zimmer, Inc. | The associated product labeling does not adequately provide compatibility information for use of the 22.2 mm Diameter Ceramic Femoral Heads with cobalt-chrome f |
| 2025-03-24 | Zimmer, Inc. | The associated product labeling does not adequately provide compatibility information for use of the 22.2 mm Diameter Ceramic Femoral Heads with cobalt-chrome f |
| 2025-02-12 | Zimmer, Inc. | There is a potential design issue with the Z1 Offset Stem Inserter leading to fracturing of the distal tip. |
| 2024-12-05 | Waldemar Link GmbH & Co. KG (Mfg Site) | Error on the main label and the patient label. The labels indicate a size XXL, this is a standard-size neck segment.. All further information on the labels is c |
| 2024-08-08 | Zimmer GmbH | Mislabeled: Incorrect sleeve in the packaging. The outer packaging is labeled as a standard neck sleeve, however, the product within the box is a -6mm neck slee |
| 2024-08-08 | Zimmer GmbH | Mislabeled: Incorrect sleeve in the packaging. The outer packaging is labeled as a standard neck sleeve, however, the product within the box is a -6mm neck slee |
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