Aesthetic Lasers, Inc.
Country not established
- Devices
- 1
What Aesthetic Lasers, Inc. makes
Aesthetic Lasers, Inc. manufactures the DMS-1000C Dermoabrader, a device designed for controlled skin resurfacing and exfoliation procedures.
The DMS-1000C Dermoabrader is classified as a Class I medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Dms-1000C Dermoabrader Ref K963204
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aesthetic Lasers, Inc. have in the registry?
The registry currently lists 1 device for Aesthetic Lasers, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aesthetic Lasers, Inc.'s devices?
Among its 1 most recently registered device, Aesthetic Lasers, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Aesthetic Lasers, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Aesthetic Lasers, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Aesthetic Lasers, Inc. in the registry?
The most recently registered devices listed for Aesthetic Lasers, Inc. include DMS-1000C DERMOABRADER.