BodyFX AS600874A
BodyFX AS600874A is a Class II device made by Inmode MD, Ltd., cleared under FDA 510(k) K131362 on 8 Oct 2013 and listed in FDA GUDID since 25 Oct 2016 (UDI-DI 07290016633085), 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 | Number07290016633085 | Date25 Oct 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK131362 | Date8 Oct 2013 | StatusActive |
Official records
- AccessGUDID record 07290016633085
- FDA 510(k) database K131362
Across registries
- FDA 510(k) K131362 decided 8 Oct 2013 Active
- FDA GUDID UDI-DI 07290016633085 listed 25 Oct 2016 Listed
Timeline
- Cleared FDA 510(k) K131362
- Listed FDA GUDID 07290016633085
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- BodyFX
- Generic name
- Radio-frequency skin surface treatment system
- Model / Ref / Catalog
- AS600874A
- Primary DI / UDI-DI
- 07290016633085
- 510(k) Number
- FDA product code
- NUV, ISA
- GMDN term
- Radio-frequency skin surface treatment system
- Device class
- Class II
- Regulation number
- 878.4810, 890.5660
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Radio-frequency skin surface treatment system.