Dark Star Deformity 101199
Dark Star Deformity 101199 (DS0078-L) is a Class II device made by Republic Spine, LLC, cleared under FDA 510(k) K223096 on 26 May 2023 and listed in FDA GUDID since 18 Nov 2025 (UDI-DI B0751011990), 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 | NumberB0751011990 | Date18 Nov 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK223096 | Date26 May 2023 | StatusActive |
Official records
- FDA 510(k) database K223096
Across registries
- FDA 510(k) K223096 decided 26 May 2023 Active
- FDA GUDID UDI-DI B0751011990 listed 18 Nov 2025 Listed
Timeline
- Cleared FDA 510(k) K223096
- Listed FDA GUDID B0751011990
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Dark Star Deformity
- Generic name
- Manual orthopaedic bender, reusable
- Model / Ref / Catalog
- 101199, DS0078-L
- Primary DI / UDI-DI
- B0751011990
- 510(k) Number
- FDA product code
- NKB, KWP
- GMDN term
- Manual orthopaedic bender, reusable
- Device class
- Class II
- Regulation number
- 888.3070, 888.3050
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- MRI safety
- MR Unsafe