Sleds MMSLED-42
by Trimed, INC.
Sleds MMSLED-42 is a Class II device made by Trimed, INC., cleared under FDA 510(k) K243999 on 19 Mar 2025 and listed in FDA GUDID since 7 Sep 2016 (UDI-DI 00842188109058), 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 | NumberK243999 | Date19 Mar 2025 | StatusActive |
| United States | GUDID listing | Number00842188109058 | Date7 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00842188109058
- FDA 510(k) database K243999
Across registries
- FDA 510(k) K243999 decided 19 Mar 2025 Active
- FDA GUDID UDI-DI 00842188109058 listed 7 Sep 2016 Listed
Timeline
- Listed FDA GUDID 00842188109058
- Cleared FDA 510(k) K243999
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Sleds
- Generic name
- Orthopaedic bone pin, non-bioabsorbable
- Model / Ref / Catalog
- MMSLED-42
- Primary DI / UDI-DI
- 00842188109058
- 510(k) Number
- FDA product code
- NDL
- GMDN term
- Orthopaedic bone pin, non-bioabsorbable
- Device class
- Class II
- Regulation number
- 888.3040
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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