Trophy Skin REJUVATONEMD
Trophy Skin REJUVATONEMD is a Class II device made by Trophy Skin, Inc., cleared under FDA 510(k) K152199 on 23 Mar 2016 and listed in FDA GUDID since 31 Jan 2020 (UDI-DI 00851561006105), 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 | Number00851561006105 | Date31 Jan 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK152199 | Date23 Mar 2016 | StatusActive |
Official records
- AccessGUDID record 00851561006105
- FDA 510(k) database K152199
Across registries
- FDA 510(k) K152199 decided 23 Mar 2016 Active
- FDA GUDID UDI-DI 00851561006105 listed 31 Jan 2020 Listed
Timeline
- Cleared FDA 510(k) K152199
- Listed FDA GUDID 00851561006105
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Trophy Skin
- Generic name
- Hand-held deep-tissue electromagnetic stimulator
- Model / reference
- REJUVATONEMD
- Primary DI / UDI-DI
- 00851561006105
- 510(k) Number
- FDA product code
- NFO
- GMDN term
- Hand-held deep-tissue electromagnetic stimulator
- Device class
- Class II
- Regulation number
- 882.5890
- GUDID distribution status
- In Commercial Distribution
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