Stryker 48252106
by Tedan Surgical Innovations, L.L.C.
Stryker 48252106 is a Class II device made by Tedan Surgical Innovations, L.L.C., cleared under FDA 510(k) K093792 on 18 Mar 2010 and listed in FDA GUDID since 1 Dec 2017 (UDI-DI 00843059116694), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00843059116694 | Date1 Dec 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK093792 | Date18 Mar 2010 | StatusActive |
Official records
- AccessGUDID record 00843059116694
- FDA 510(k) database K093792
Across registries
- FDA 510(k) K093792 decided 18 Mar 2010 Active
- FDA GUDID UDI-DI 00843059116694 listed 1 Dec 2017 Listed
Timeline
- Cleared FDA 510(k) K093792
- Listed FDA GUDID 00843059116694
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Stryker
- Generic name
- General-purpose light source
- Model / reference
- 48252106
- Primary DI / UDI-DI
- 00843059116694
- 510(k) Number
- FDA product code
- FCW
- GMDN term
- General-purpose light source
- Device class
- Class II
- Regulation number
- 876.1500
- GUDID distribution status
- In Commercial Distribution
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