Tandry CMF Plate System T50-12907
by Microware Precision Co., Ltd.
Tandry CMF Plate System T50-12907 is a Class II device made by Microware Precision Co., Ltd., cleared under FDA 510(k) K220360 on 10 Nov 2022 and listed in FDA GUDID since 29 Apr 2026 (UDI-DI 04719873108190), 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 | Number04719873108190 | Date29 Apr 2026 | StatusListed |
| United States | FDA 510(k)SESE | NumberK220360 | Date10 Nov 2022 | StatusActive |
Official records
- AccessGUDID record 04719873108190
- FDA 510(k) database K220360
Across registries
- FDA 510(k) K220360 decided 10 Nov 2022 Active
- FDA GUDID UDI-DI 04719873108190 listed 29 Apr 2026 Listed
Timeline
- Cleared FDA 510(k) K220360
- Listed FDA GUDID 04719873108190
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Tandry CMF Plate System
- Generic name
- Craniofacial bone screw, non-bioabsorbable
- Model / reference
- T50-12907
- Primary DI / UDI-DI
- 04719873108190
- 510(k) Number
- FDA product code
- DZL
- GMDN term
- Craniofacial bone screw, non-bioabsorbable
- Device class
- Class II
- Regulation number
- 872.4880
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization