Plexr Plus M
by Gmv SRL
Plexr Plus M is a thermo-mechanical skin surface treatment system (FDA Class II; FDA product code GEI, Electrosurgical, Cutting & Coagulation & Accessories) made by Gmv SRL, cleared under FDA 510(k) K210693 on 22 Mar 2022 and listed in FDA GUDID since 10 Jan 2024 (UDI-DI 08057506440092), 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 | Number08057506440092 | Date10 Jan 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK210693 | Date22 Mar 2022 | StatusActive |
Official records
- AccessGUDID record 08057506440092
- FDA 510(k) database K210693
Across registries
- FDA 510(k) K210693 decided 22 Mar 2022 Active
- FDA GUDID UDI-DI 08057506440092 listed 10 Jan 2024 Listed
Timeline
- Cleared FDA 510(k) K210693
- Listed FDA GUDID 08057506440092
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Plexr Plus
- Generic name
- Thermo-mechanical skin surface treatment system
- Model / reference
- PLEXR PLUS M
- Primary DI / UDI-DI
- 08057506440092
- 510(k) Number
- FDA product code
- GEI
- GMDN term
- Thermo-mechanical skin surface treatment system
- Device class
- Class II
- Regulation number
- 878.4400
- GUDID distribution status
- In Commercial Distribution
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