Encore Medical, L.P. - FDA 510(k) Cleared Devices
81
Total
81
Cleared
0
Denied
Encore Medical, L.P. has 81 FDA 510(k) cleared orthopedic devices. Based in Austin, US.
Latest FDA clearance: Jan 2026. Active since 2002.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Encore Medical, L.P.
81 devices
Cleared
Jan 15, 2026
AltiVate Reverse® ADLC Glenosphere
Orthopedic
154d
Cleared
Dec 19, 2025
EMPOWR Knee
Orthopedic
93d
Cleared
Nov 12, 2025
EMPOWR Acetabular® Liner Extension
Orthopedic
149d
Cleared
Aug 05, 2025
AltiVate Reverse® Glenoid
Orthopedic
28d
Cleared
Jul 08, 2025
EMPOWR Revision Knee™ (EMPOWR Revision VVC+, e+ Tibial Insert)
Orthopedic
28d
Cleared
Jul 02, 2025
EMPOWR Revision Knee™ (EMPOWR Revision Knee™ Symmetric TT Cones)
Orthopedic
71d
Cleared
May 16, 2025
AltiVate Reverse Shoulder System
Orthopedic
30d
Cleared
Feb 07, 2025
ceramys™ femoral head system
Orthopedic
259d
Cleared
May 29, 2024
AltiVate Reverse® Glenoid
Orthopedic
216d
Cleared
Jun 23, 2023
AltiVate® Anatomic Shoulder AG e+™ with Markers
Orthopedic
301d
Cleared
Jul 07, 2022
AltiVate® Anatomic Shoulder AG e+™ with Markers
Orthopedic
266d
Cleared
Apr 01, 2022
EMPOWR Revision Knee
Orthopedic
116d
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