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Encore Medical, L.P.

United Statesfrom the FDA registration address FDA establishment FEI 1000116912

Encore Medical, L.P. is a medical device manufacturer, with 80 devices listed in FDA 510(k) (FDA Class II and III) as of 12 Nov 2026.

Devices
80
Registrations
FDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 12 Nov 2026

Registries
  • FDA 510(k) 80
Device classes
  • FDA Class II 75
  • FDA Class III 5
Identifiers
  • FDA FEI 1000116912

What Encore Medical, L.P. makes

The company designs and manufactures orthopaedic implants and surgical tools, including modular hip and shoulder prostheses, knee replacements (both cruciate-retaining and posterior-stabilized), tibial inserts, and reusable positioning instruments for joint surgeries. Their portfolio also covers polyethylene acetabular liners and implant templates to assist in precise surgical alignment.

These devices are regulated under the FDA’s classification system as Class I, Class II, or Class III, depending on risk level, and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue80

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Company details

FDA FEI number
1000116912
Address
9800 METRIC BLVD., AUSTIN, TX, 78758

Frequently asked questions

How many devices does ENCORE MEDICAL, L.P. have in the registry?

The registry currently lists 80 devices for ENCORE MEDICAL, L.P.. Devices recorded under merged duplicate company entries are counted once.

Which registries list ENCORE MEDICAL, L.P.'s devices?

Among its 50 most recently registered devices, ENCORE MEDICAL, L.P. has devices listed in FDA 510(k) (50 devices).

What risk classes do ENCORE MEDICAL, L.P.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for ENCORE MEDICAL, L.P.'s devices are Class II and Class III. Each device page shows its own class and authorisation.

What are the newest devices from ENCORE MEDICAL, L.P. in the registry?

The most recently registered devices listed for ENCORE MEDICAL, L.P. include REVERSE SHOULDER PROSTHESIS MONOBLOCK HEMI ADAPTER, AltiVate Anatomic Canal-Sparing (CS) Shoulder, TAPERFILL FEMORAL HIP STEM 425-31-005_017 425-41-005_019 and EMPOWR Universal Tibial Baseplate.

Generated automatically from registry data and not verified by a human reviewer.

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.