MiniFX AG604696A
MiniFX AG604696A is a Class II device made by Inmode MD, Ltd., cleared under FDA 510(k) K160329 on 19 Aug 2016 and listed in FDA GUDID since 25 Oct 2016 (UDI-DI 07290016633238), 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 | Number07290016633238 | Date25 Oct 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK160329 | Date19 Aug 2016 | StatusActive |
Official records
- AccessGUDID record 07290016633238
- FDA 510(k) database K160329
Across registries
- FDA 510(k) K160329 decided 19 Aug 2016 Active
- FDA GUDID UDI-DI 07290016633238 listed 25 Oct 2016 Listed
Timeline
- Cleared FDA 510(k) K160329
- Listed FDA GUDID 07290016633238
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- MiniFX
- Generic name
- Radio-frequency skin surface treatment system
- Model / Ref / Catalog
- AG604696A
- Primary DI / UDI-DI
- 07290016633238
- 510(k) Number
- FDA product code
- GEI, PBX
- GMDN term
- Radio-frequency skin surface treatment system
- Device class
- Class II
- Regulation number
- 878.4400
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Radio-frequency skin surface treatment system.