Prosthesis, Knee, Femorotibial, Non-constrained, Cemented, Metal/polymer
Orthopedic · 21 CFR 888.3520
Recent MDR events
2,520 adverse event reports on file
- Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/PolymerJul 27, 2026InjurySmith & Nephew, Inc.1020279-2026-01014
- Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/PolymerJul 27, 2026InjurySmith & Nephew, Inc.1020279-2026-01017
- Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/PolymerJul 27, 2026InjurySmith & Nephew, Inc.1020279-2026-01024
- PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMERJul 22, 2026InjurySmith & Nephew, Inc.1020279-2026-01011
- PSN PK VE PLY LM SZ G 8MMJul 17, 2026InjuryZimmer Biomet, Inc.0001822565-2026-02604
- PSN PK CMT TIB LM SZ GJul 17, 2026InjuryZimmer Orthopaedic Mfg. Ltd.3007963827-2026-00306
- PSN PK CMT FEM LM SZ 4Jul 17, 2026InjuryZimmer Orthopaedic Mfg. Ltd.3007963827-2026-00307
- MG UNI FEM PRC RT M/LT L LGE+Jul 16, 2026InjuryZimmer Biomet, Inc.0001822565-2026-02585
- MOTO PARTIAL KNEE SYSTEM - MEDIALJul 14, 2026InjuryMedacta International Sa3005180920-2026-00696
- MOTO PARTIAL KNEE SYSTEM - MEDIALJul 14, 2026MalfunctionMedacta International Sa3005180920-2026-00730
Event type breakdown
Recalls
104 recall events for this product code
- Smith & Nephew, Inc.Open, ClassifiedMay 31, 2023
Smith&Nephew ENGAGE Cementless Partial Knee System, Porous Femoral components, Part Numbers:
Recent complaint data indicates that the revision rate may be trending higher than corresponding similar devices in global joint replacement registries. The data identifies a potential signal that the performance is an outlier versus the state of the art with respect to the risk for revision.
Z-1670-2023 · View FDA record ↗ - Smith & Nephew, Inc.Open, ClassifiedMay 31, 2023
Smith&Nephew ENGAGE Cementless Partial Knee System, Tibial Anchor Stem, Part Numbers: a) REF 1-10011-100 (SIZE 1-2), b) REF 1-10011-200 (SIZE 3-4), c) REF 1
Recent complaint data indicates that the revision rate may be trending higher than corresponding similar devices in global joint replacement registries. The data identifies a potential signal that the performance is an outlier versus the state of the art with respect to the risk for revision.
Z-1671-2023 · View FDA record ↗ - Smith & Nephew, Inc.Open, ClassifiedMay 31, 2023
Smith&Nephew ENGAGE Cementless Partial Knee System, Coated Tibial Tray, Part Numbers: a) REF 1-10012-100, SIZE 1-LEFT MEDIAL;
Recent complaint data indicates that the revision rate may be trending higher than corresponding similar devices in global joint replacement registries. The data identifies a potential signal that the performance is an outlier versus the state of the art with respect to the risk for revision.
Z-1672-2023 · View FDA record ↗ - Smith & Nephew, Inc.Open, ClassifiedMay 31, 2023
Smith&Nephew ENGAGE Cementless Partial Knee System, Coated Tibial Insert, Part Numbers:
Recent complaint data indicates that the revision rate may be trending higher than corresponding similar devices in global joint replacement registries. The data identifies a potential signal that the performance is an outlier versus the state of the art with respect to the risk for revision.
Z-1673-2023 · View FDA record ↗ - Linkbio Corp.Open, ClassifiedMay 4, 2023
LINK SLED Knee System:
Additional Label Warnings: Amendment / reinforcement of the Surgical Technique and future product training on the updated technique, due to early aseptic loosening or increased wear of the implant caused by suboptimal positioning of the implant or inadequate cementing technique leading to an unsatisfactory surgical result, and in the worst case, intervention or revision earlier than expected
Z-1507-2023 · View FDA record ↗ - Linkbio Corp.Open, ClassifiedMay 4, 2023
LINK SLED Knee System:
Additional Label Warnings: Amendment / reinforcement of the Surgical Technique and future product training on the updated technique, due to early aseptic loosening or increased wear of the implant caused by suboptimal positioning of the implant or inadequate cementing technique leading to an unsatisfactory surgical result, and in the worst case, intervention or revision earlier than expected
Z-1508-2023 · View FDA record ↗ - Linkbio Corp.Open, ClassifiedMay 4, 2023
LINK SLED Knee System:
Additional Label Warnings: Amendment / reinforcement of the Surgical Technique and future product training on the updated technique, due to early aseptic loosening or increased wear of the implant caused by suboptimal positioning of the implant or inadequate cementing technique leading to an unsatisfactory surgical result, and in the worst case, intervention or revision earlier than expected
Z-1509-2023 · View FDA record ↗ - Linkbio Corp.Open, ClassifiedMay 4, 2023
LINK SLED Knee System:
Additional Label Warnings: Amendment / reinforcement of the Surgical Technique and future product training on the updated technique, due to early aseptic loosening or increased wear of the implant caused by suboptimal positioning of the implant or inadequate cementing technique leading to an unsatisfactory surgical result, and in the worst case, intervention or revision earlier than expected
Z-1510-2023 · View FDA record ↗ - Linkbio Corp.Open, ClassifiedMay 4, 2023
LINK SLED Knee System:
Additional Label Warnings: Amendment / reinforcement of the Surgical Technique and future product training on the updated technique, due to early aseptic loosening or increased wear of the implant caused by suboptimal positioning of the implant or inadequate cementing technique leading to an unsatisfactory surgical result, and in the worst case, intervention or revision earlier than expected
Z-1511-2023 · View FDA record ↗ - Linkbio Corp.Open, ClassifiedMay 4, 2023
LINK SLED Knee System:
Additional Label Warnings: Amendment / reinforcement of the Surgical Technique and future product training on the updated technique, due to early aseptic loosening or increased wear of the implant caused by suboptimal positioning of the implant or inadequate cementing technique leading to an unsatisfactory surgical result, and in the worst case, intervention or revision earlier than expected
Z-1512-2023 · View FDA record ↗
Registered firms
481 firms currently registered for this product code
Conformis, Inc.
Wilmington, MA, US
Engineered Medical Systems, Llc
Bartlett, TN, US
Ppd Meditech, Div. Of Industries Ppd Inc.
Waterville Quebec, CA
Intai Technology Corp. Implants Business Unit
Taichung City, TW
Materialise Usa, Llc.
Plymouth, MI, US
Smith & Nephew, Inc.
MEMPHIS, TN, US
Isomedix Operations Inc.
Sandy, UT, US
Symmetry Medical Manufacturing Inc
CLAYPOOL, IN, US
Arthrex Manufacturing Inc.
Pendleton, SC, US
Straits Orthopaedics (mfg) Sdn Bhd
Bandar Cassia Pulau Pinang, MY
Blue Belt Technologies, Inc.
Pittsburgh, PA, US
Arvato Usa Llc
Memphis, TN, US
Paragon Medical Device (changzhou) Co., Ltd.
Changzhou Jiangsu, CN
Watershed Idea Foundry, Inc.
Carlsbad, CA, US
Biomet Chile S.a.
Santiago de Chile Region Metropolitana, CL
Sterilization Services Of Georgia, Inc.
ATLANTA, GA, US
Symmetry Medical Manufacturing Inc.
WARSAW, IN, US
Arthrex Distribution Hub Emea B.v.
Venlo Limburg, NL
Zimmer Biomet Taiwan Co., Ltd.
Taipei, TW
Structure Medical, Llc.
Mooresville, NC, US
Signature Orthopaedics Pty Limited
Sydney New South Wales, AU
Almark Tool & Manufacturing Company, Inc.
Garwood, NJ, US
510(k) clearances
115 clearances for this product code
- Shalby Advanced Technologies, Inc. Dba Consensus OrthopedicsApr 2, 2026
K260796 · Tahoe Unicondylar Knee System with TiNbN Overcoat
- Signature Orthopaedics Pty, Ltd.Dec 16, 2025
K251771 · Cambridge Partial Knee
- Zimmer BiometAug 15, 2025
K251834 · Persona Partial Knee
- Medacta International S.A.Jul 24, 2025
K251618 · MOTO Partial Knee System Extension
- Arthrex, Inc.Jul 1, 2025
K251453 · Arthrex iBalance Partial Knee System
- Globus Medical, Inc.Dec 6, 2024
K241260 · ACTIFY Unicondylar Knee System
- Smith & Nephew, Inc.Oct 30, 2024
K242711 · JOURNEY II Unicompartmental Knee System (JOURNEY II UK)
- Overture OrthopaedicsOct 7, 2024
K242746 · OvertureTi Knee Resurfacing SystemTM