Secret PRO Main Unit FRX-C2
by CLASSYS Inc.
Secret PRO Main Unit FRX-C2 is a Class II device made by CLASSYS Inc., cleared under FDA 510(k) K233374 on 14 Dec 2023 and listed in FDA GUDID since 31 Oct 2024 (UDI-DI 08800016903690), 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 | Number08800016903690 | Date31 Oct 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK233374 | Date14 Dec 2023 | StatusActive |
Official records
- AccessGUDID record 08800016903690
- FDA 510(k) database K233374
Across registries
- FDA 510(k) K233374 decided 14 Dec 2023 Active
- FDA GUDID UDI-DI 08800016903690 listed 31 Oct 2024 Listed
Timeline
- Cleared FDA 510(k) K233374
- Listed FDA GUDID 08800016903690
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Secret PRO Main Unit
- Generic name
- Dermatological carbon dioxide laser system
- Model / reference
- FRX-C2
- Primary DI / UDI-DI
- 08800016903690
- 510(k) Number
- FDA product code
- GEI, GEX, OUH
- GMDN term
- Dermatological carbon dioxide laser system
- Device class
- Class II
- Regulation number
- 878.4400, 878.4810
- GUDID distribution status
- In Commercial Distribution
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