Identity
- Trade Name
- DJO SURGICAL FDA UDI
- Generic Name
- Total reverse shoulder prosthesis FDA UDI
- Device Name
- SOCKET, INSERT, 44MM, STD FDA UDI
- Model / Reference
- 508-00-044 FDA UDI
- Description
- SOCKET, INSERT, 44MM, STD FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00888912024662 FDA UDI
- FDA Product Code
- KWS FDA UDI
- GMDN Term
- Total reverse shoulder prosthesis FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3660 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
No
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Total reverse shoulder prosthesis
Djo Surgical by Encore Medical, L.p. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Total reverse shoulder prosthesis.
- Anatomical Shoulder# — Zimmer, Inc. · Class II
- Arthrex® — Arthrex, Inc. · Class II
- Arthrex® — Arthrex, Inc. · Class II
- Shoulder Innovations Inset Reverse Total Shoulder — SHOULDER INNOVATIONS, Inc · Class II
- R1 Reverse Shoulder System — CATALYST ORTHOSCIENCE Inc · Class II
- DELTA XTEND — DEPUY (IRELAND) · Class II
- Tornier Flex Shoulder System — TORNIER, INC. · Class II
- AEQUALIS REVERSED FRACTURE — TORNIER, INC. · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Encore Medical, L.p.
Sources (1)
- FDA UDI a1050182-bb31-4d51-97e4-a7380d03236e 33 fields · synced May 30, 2026