Silk'n Titan AllWays
Silk'n Titan AllWays (7290019840008) is a medical device (FDA Class II) made by Silkn Beauty Ltd., cleared under FDA 510(k) K230013 on 30 Aug 2023 and listed in FDA GUDID since 14 Sep 2023 (UDI-DI 17290019840005), 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 | Number17290019840005 | Date14 Sep 2023 | StatusListed |
| United States | FDA 510(k)SESE | NumberK230013 | Date30 Aug 2023 | StatusActive |
Official records
- AccessGUDID record 17290019840005
- FDA 510(k) database K230013
Across registries
- FDA 510(k) K230013 decided 30 Aug 2023 Active
- FDA GUDID UDI-DI 17290019840005 listed 14 Sep 2023 Listed
Timeline
- Cleared FDA 510(k) K230013
- Listed FDA GUDID 17290019840005
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Silk'n
- Generic name
- Radio-frequency skin surface treatment system applicator
- Model / Ref / Catalog
- Titan AllWays, 7290019840008
- Primary DI / UDI-DI
- 17290019840005
- 510(k) Number
- FDA product code
- PAY, OHS
- GMDN term
- Radio-frequency skin surface treatment system applicator
- Device class
- Class II
- Regulation number
- 878.4420, 878.4810
- GUDID distribution status
- In Commercial Distribution