Vision Pro, LLC
Country not established
- Devices
- 1
What Vision Pro, LLC makes
Vision Pro, LLC manufactures the LAFACI, a laser-assisted facial rejuvenation device designed for non-ablative skin resurfacing to improve texture and tone through controlled thermal remodeling.
The company’s portfolio is regulated under FDA Class II devices, with the LAFACI authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) database. Vision Pro, LLC is based in the United States.
Catalogue
Lafaci Ref K032400
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vision Pro, LLC have in the registry?
The registry currently lists 1 device for Vision Pro, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vision Pro, LLC's devices?
Among its 1 most recently registered device, Vision Pro, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Vision Pro, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Vision Pro, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vision Pro, LLC in the registry?
The most recently registered devices listed for Vision Pro, LLC include LAFACI.