N-Force Blue ™ IN050-8
by Etex Corp.
N-Force Blue ™ IN050-8 is a Class II device made by Etex Corp., cleared under FDA 510(k) K141245 on 9 Jul 2014 and listed in FDA GUDID since 16 Dec 2019 (UDI-DI 00889024563285), active as of 22 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 | Number00889024563285 | Date16 Dec 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK141245 | Date9 Jul 2014 | StatusActive |
Official records
- AccessGUDID record 00889024563285
- FDA 510(k) database K141245
Across registries
- FDA 510(k) K141245 decided 9 Jul 2014 Active
- FDA GUDID UDI-DI 00889024563285 listed 16 Dec 2019 Listed
Timeline
- Cleared FDA 510(k) K141245
- Listed FDA GUDID 00889024563285
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- N-Force Blue ™
- Generic name
- Bone graft delivery kit
- Model / Ref / Catalog
- IN050-8
- Primary DI / UDI-DI
- 00889024563285
- 510(k) Number
- FDA product code
- FMF
- GMDN term
- Bone graft delivery kit
- Device class
- Class II
- Regulation number
- 880.5860
- GUDID distribution status
- In Commercial Distribution
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