Techfit 0
by Techfit Digital Surgery, Inc. 45 variants
Techfit 0 (MAPMMCL), a custom-made organ/bone anatomy model (FDA Class II; FDA product code LLZ, System, Image Processing, Radiological) made by Techfit Digital Surgery, Inc., was cleared under FDA 510(k) K222577 on 6 Jan 2023 and listed in FDA GUDID on 9 Jun 2023 (UDI-DI 00860007543432); the registry lists it as not in commercial distribution (GUDID) 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 | Number00860007543432 | Date9 Jun 2023 | StatusListed |
| United States | FDA 510(k)SESE | NumberK222577 | Date6 Jan 2023 | StatusActive |
Official records
- AccessGUDID record 00860007543432
- FDA 510(k) database K222577
Across registries
- FDA 510(k) K222577 decided 6 Jan 2023 Active
- FDA GUDID UDI-DI 00860007543432 listed 9 Jun 2023 Listed
Timeline
- Cleared FDA 510(k) K222577
- Listed FDA GUDID 00860007543432
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Techfit
- Generic name
- Custom-made organ/bone anatomy model
- Model / Ref / Catalog
- 0, MAPMMCL
- Primary DI / UDI-DI
- 00860007543432
- 510(k) Number
- FDA product code
- LLZ
- GMDN term
- Custom-made organ/bone anatomy model
- Device class
- Class II
- Regulation number
- 892.2050
- GUDID distribution status
- Not in Commercial Distribution
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