VLaze Applicator AG605988A
VLaze Applicator AG605988A is a Class II device made by Inmode MD, Ltd., cleared under FDA 510(k) K221571 on 30 Jun 2022 (1 earlier submission) and listed in FDA GUDID since 2 Nov 2022 (UDI-DI 07290016633290), 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 | Number07290016633290 | Date2 Nov 2022 | StatusListed |
| United States | FDA 510(k)SESE | NumberK221571 | Date30 Jun 2022 | StatusActive |
Official records
- AccessGUDID record 07290016633290
- FDA 510(k) database K221571
- FDA 510(k) database K173677
Across registries
- FDA 510(k) K221571 decided 30 Jun 2022 Active
- FDA GUDID UDI-DI 07290016633290 listed 2 Nov 2022 Listed
Timeline
- Cleared FDA 510(k) K173677
- Cleared FDA 510(k) K221571
- Listed FDA GUDID 07290016633290
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- VLaze Applicator
- Generic name
- Multi-modality skin surface treatment system
- Model / Ref / Catalog
- AG605988A
- Primary DI / UDI-DI
- 07290016633290
- FDA product code
- GEX
- GMDN term
- Multi-modality skin surface treatment system
- Device class
- Class II
- Regulation number
- 878.4810
- GUDID distribution status
- In Commercial Distribution
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