286005324N
286005324N is a Class II device made by Medos International Sàrl, cleared under FDA 510(k) K233254 on 14 Jun 2024 (1 earlier submission) and listed in FDA GUDID since 9 Aug 2022 (UDI-DI 10705034548876), 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 | FDA 510(k)SESE | NumberK233254 | Date14 Jun 2024 | StatusActive |
| United States | GUDID listing | Number10705034548876 | Date9 Aug 2022 | StatusListed |
Official records
- AccessGUDID record 10705034548876
- FDA 510(k) database K233254
- FDA 510(k) database K212756
Across registries
- FDA 510(k) K233254 decided 14 Jun 2024 Active
- FDA GUDID UDI-DI 10705034548876 listed 9 Aug 2022 Listed
Timeline
- Cleared FDA 510(k) K212756
- Listed FDA GUDID 10705034548876
- Cleared FDA 510(k) K233254
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Generic name
- Bone curette, reusable
- Model / Ref / Catalog
- 286005324N
- Primary DI / UDI-DI
- 10705034548876
- FDA product code
- OLO
- GMDN term
- Bone curette, reusable
- Device class
- Class II
- Regulation number
- 882.4560
- GUDID distribution status
- In Commercial Distribution