Encore Medical L.P.
FDA 510(k) & PMA Approved Devices — 31 products
Total Devices31
Categories10
Latest Approval2026-01-15
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K252567 | AltiVate Reverse® ADLC Glenosphere | PHX | 2026-01-15 | View |
| 510(k) | K252974 | EMPOWR Knee | JWH | 2025-12-19 | View |
| 510(k) | K251833 | EMPOWR Acetabular® Liner Extension | LPH | 2025-11-12 | View |
| 510(k) | K252141 | AltiVate Reverse® Glenoid | PHX | 2025-08-05 | View |
| 510(k) | K251776 | EMPOWR Revision Knee (EMPOWR Revision VVC+, e+ Tibial Insert) | JWH | 2025-07-08 | View |
| 510(k) | K251241 | EMPOWR Revision Knee (EMPOWR Revision Knee Symmetric TT Cones) | JWH | 2025-07-02 | View |
| 510(k) | K251184 | AltiVate Reverse Shoulder System; RSP Shoulder System; SMR Shoulder System; PRIMA Humeral System; PRIMA Glenoid System | PHX | 2025-05-16 | View |
| 510(k) | K241483 | ceramys femoral head system | LZO | 2025-02-07 | View |
| 510(k) | K233481 | AltiVate Reverse® Glenoid | PHX | 2024-05-29 | View |
| 510(k) | K222592 | AltiVate® Anatomic Shoulder AG e+ with Markers | KWS | 2023-06-23 | View |
| 510(k) | K213387 | AltiVate® Anatomic Shoulder AG e+ with Markers | KWS | 2022-07-07 | View |
| 510(k) | K213793 | EMPOWR Revision Knee | JWH | 2022-04-01 | View |
| 510(k) | K210308 | EMPOWR Porous Femur with HAnano SurfaceTM | MBH | 2021-03-30 | View |
| 510(k) | K203557 | EMPOWR Dual Mobility Metal Liner, EMPOWR Dual Mobility Poly Bearing | LPH | 2021-02-10 | View |
| 510(k) | K203026 | AltiVate® Anatomic Pegged Glenoid with Markers | KWS | 2020-12-23 | View |
| 510(k) | K193226 | AltiVate Anatomic Canal-Sparing (CS) Shoulder | PKC | 2020-06-03 | View |
| 510(k) | K191325 | EMPOWR Partial Knee | HSX | 2019-07-16 | View |
| 510(k) | K190057 | DJO Acetabular System | LPH | 2019-06-07 | View |
| 510(k) | K190290 | AltiVate Reverse Humeral Stem, 48mm | KWS | 2019-04-26 | View |
| 510(k) | K180930 | EMPOWR VVC TIBIAL INSERT | JWH | 2018-07-09 | View |
No matching devices.
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