InMode AG606666A
InMode AG606666A is a multi-modality skin surface treatment system (FDA Class II) made by Inmode MD, Ltd., cleared under FDA 510(k) K240017 on 13 Jun 2024 (1 earlier submission) and listed in FDA GUDID since 14 Mar 2017 (UDI-DI 07290016633252), 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 | FDA 510(k)SESE | NumberK240017 | Date13 Jun 2024 | StatusActive |
| United States | GUDID listing | Number07290016633252 | Date14 Mar 2017 | StatusListed |
Official records
- AccessGUDID record 07290016633252
- FDA 510(k) database K240017
- FDA 510(k) database K123682
Across registries
- FDA 510(k) K240017 decided 13 Jun 2024 Active
- FDA GUDID UDI-DI 07290016633252 listed 14 Mar 2017 Listed
Timeline
- Cleared FDA 510(k) K123682
- Listed FDA GUDID 07290016633252
- Cleared FDA 510(k) K240017
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- InMode
- Generic name
- Multi-modality skin surface treatment system
- Model / Ref / Catalog
- AG606666A
- Primary DI / UDI-DI
- 07290016633252
- FDA product code
- GEX, GEI
- GMDN term
- Multi-modality skin surface treatment system
- Device class
- Class II
- Regulation number
- 878.4810, 878.4400
- GUDID distribution status
- In Commercial Distribution
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