Level One Cmf 25-887-17-09
Level One Cmf 25-887-17-09 is a Class II device made by KLS-Martin L.P., listed in FDA GUDID since 24 Mar 2016 (UDI-DI 10888118048520), 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 | Number10888118048520 | Date24 Mar 2016 | StatusListed |
Official records
- AccessGUDID record 10888118048520
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Level One Cmf
- Generic name
- Craniofacial bone screw, non-bioabsorbable
- Model / reference
- 25-887-17-09
- Primary DI / UDI-DI
- 10888118048520
- FDA product code
- MQN
- GMDN term
- Craniofacial bone screw, non-bioabsorbable
- Device class
- Class II
- Regulation number
- 872.4760
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- MRI safety
- MR Conditional
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