Gmv SRL
Country not established
Gmv SRL is a medical device manufacturer, with 3 devices listed in FDA GUDID (FDA Class II) as of 15 Nov 2026.
- Devices
- 3
Registry facts
- Registries
- FDA GUDID 3
- Device classes
- FDA Class II 3
- Identifiers
- DUNS 429475113
What Gmv SRL makes
GMV SRL manufactures thermo-mechanical skin surface treatment systems designed for controlled tissue modification. Their primary device, the PLEXR PLUS, is used for procedures such as skin resurfacing and scar revision through precise thermal and mechanical action.
The company’s portfolio is regulated under FDA Class II devices and is listed in the FDA’s Unique Device Identifier (UDI) database.
Catalogue
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
Company details
- DUNS number
- 429475113
Frequently asked questions
How many devices does GMV SRL have in the registry?
The registry currently lists 3 devices for GMV SRL. Devices recorded under merged duplicate company entries are counted once.
Which registries list GMV SRL's devices?
Among its 3 most recently registered devices, GMV SRL has devices listed in FDA GUDID (3 devices).
What risk classes do GMV SRL's devices fall under?
Among its 3 most recently registered devices, the classes recorded for GMV SRL's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from GMV SRL in the registry?
The most recently registered devices listed for GMV SRL include PLEXR PLUS H, PLEXR PLUS L and PLEXR PLUS M.