Reunion 5552-E-5217
Reunion 5552-E-5217 is a Class II device made by Stryker Corp., listed in FDA GUDID since 24 Sep 2015 (UDI-DI 07613327098044), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number07613327098044 | Date24 Sep 2015 | StatusListed |
Official records
- AccessGUDID record 07613327098044
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Reunion
- Generic name
- Stem-fixed metallic humeral head prosthesis
- Model / Ref / Catalog
- 5552-E-5217
- Primary DI / UDI-DI
- 07613327098044
- FDA product code
- KWS
- GMDN term
- Stem-fixed metallic humeral head prosthesis
- Device class
- Class II
- Regulation number
- 888.3660
- GUDID distribution status
- In Commercial Distribution
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