No Brand XK000696-7
No Brand XK000696-7 is a Class II device made by Smith & Nephew, Inc., listed in FDA GUDID since 6 Dec 2021 (UDI-DI 00885556867112), 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 | Number00885556867112 | Date6 Dec 2021 | StatusListed |
Official records
- AccessGUDID record 00885556867112
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- No Brand
- Generic name
- Knee tibia prosthesis trial, reusable
- Model / Ref / Catalog
- XK000696-7
- Primary DI / UDI-DI
- 00885556867112
- FDA product code
- HRY
- GMDN term
- Knee tibia prosthesis trial, reusable
- Device class
- Class II
- Regulation number
- 888.3530
- GUDID distribution status
- In Commercial Distribution
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