FaSet
by Dio Medical Co., Ltd. 227 variants
FaSet (FT.LN2.5025) is a device classified as Unclassified made by Dio Medical Co., Ltd., cleared under FDA 510(k) K180729 on 28 Jun 2018 and listed in FDA GUDID since 18 Mar 2021 (UDI-DI 08800113952430), 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 | Number08800113952430 | Date18 Mar 2021 | StatusListed |
| United States | FDA 510(k)SESE | NumberK180729 | Date28 Jun 2018 | StatusActive |
Official records
- AccessGUDID record 08800113952430
- FDA 510(k) database K180729
Across registries
- FDA 510(k) K180729 decided 28 Jun 2018 Active
- FDA GUDID UDI-DI 08800113952430 listed 18 Mar 2021 Listed
Timeline
- Cleared FDA 510(k) K180729
- Listed FDA GUDID 08800113952430
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Generic name
- Spinal fixation plate, non-bioabsorbable
- Model / Ref / Catalog
- A, FT.LN2.5025
- Primary DI / UDI-DI
- 08800113952430
- 510(k) Number
- FDA product code
- MRW
- GMDN term
- Spinal fixation plate, non-bioabsorbable
- Device class
- U
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- MRI safety
- MR Unsafe
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