Slimspec LX-5-A999b
Slimspec LX-5-A999b is a Class I device made by Medispec, Ltd., listed in FDA GUDID since 7 Jun 2023 (UDI-DI 07290016498615), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number07290016498615 | Date7 Jun 2023 | StatusListed |
Official records
- AccessGUDID record 07290016498615
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Slimspec
- Generic name
- Pressure-wave skin/body contouring system
- Model / reference
- LX-5-A999b
- Primary DI / UDI-DI
- 07290016498615
- FDA product code
- ISA
- GMDN term
- Pressure-wave skin/body contouring system
- Device class
- Class I
- Regulation number
- 890.5660
- GUDID distribution status
- In Commercial Distribution
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