Identity
- Trade Name
- ReUnion FDA UDI
- Generic Name
- Total shoulder prosthesis FDA UDI
- Device Name
- Dual Radius Humeral Head FDA UDI
- Model / Reference
- R5350-5024 FDA UDI
- Description
- Dual Radius Humeral Head FDA UDI
Identifiers
- Catalog Number
- R5350-5024 FDA UDI
- Primary DI / UDI-DI
- 07613327139532 FDA UDI
- FDA Product Code
- KWS FDA UDIHSD FDA UDI
- GMDN Term
- Total shoulder prosthesis FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3660 FDA UDI888.3690 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Total shoulder prosthesis
ReUnion by Howmedica Osteonics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Total shoulder prosthesis.
- B-P TOTAL SHOULDER SYSTEM — ENDOTEC, INC. · Class II
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- DJO SURGICAL — ENCORE MEDICAL, L.P. · Class II
- Shoulder Innovations Humeral Stemless System — SHOULDER INNOVATIONS, Inc · Class II
- Shoulder Innovations Inset Reverse Total Shoulder — SHOULDER INNOVATIONS, Inc · Class II
- Shoulder System — Medacta International · Class II
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- Arthrex® — Arthrex, Inc. · Class II
Cleared under the same submission
K955731 also covers:
- ReUnion — Howmedica Osteonics Corp.
- ReUnion — Howmedica Osteonics Corp.
- ReUnion — Howmedica Osteonics Corp.
- ReUnion — Howmedica Osteonics Corp.
- ReUnion — Howmedica Osteonics Corp.
- ReUnion — Howmedica Osteonics Corp.
- ReUnion — Howmedica Osteonics Corp.
- ReUnion — Howmedica Osteonics Corp.
- ReUnion — Howmedica Osteonics Corp.
- ReUnion — Howmedica Osteonics Corp.
- ReUnion — Howmedica Osteonics Corp.
- ReUnion — Howmedica Osteonics Corp.
K990598 also covers:
- ReUnion — Howmedica Osteonics Corp.
- ReUnion — Howmedica Osteonics Corp.
- ReUnion — Howmedica Osteonics Corp.
- ReUnion — Howmedica Osteonics Corp.
- ReUnion — Howmedica Osteonics Corp.
- ReUnion — Howmedica Osteonics Corp.
- ReUnion — Howmedica Osteonics Corp.
- ReUnion — Howmedica Osteonics Corp.
- ReUnion — Howmedica Osteonics Corp.
- ReUnion — Howmedica Osteonics Corp.
- ReUnion — Howmedica Osteonics Corp.
- ReUnion — Howmedica Osteonics Corp.
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Howmedica Osteonics Corp.
Sources (1)
- FDA UDI e0a10167-18ef-44f0-bc7b-f4ba6e7a4446 36 fields · synced May 30, 2026