Vasamed, Inc.
Country not established
- Devices
- 1
What Vasamed, Inc. makes
Vasamed, Inc. manufactures the SensiLase Pad-IQ, a diagnostic device designed for assessing skin conditions, likely through laser or light-based analysis to evaluate tissue properties.
The SensiLase Pad-IQ is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) clearance process. The company is based in the United States.
Catalogue
Sensilase Pad-Iq Ref K110438
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vasamed, Inc. have in the registry?
The registry currently lists 1 device for Vasamed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vasamed, Inc.'s devices?
Among its 1 most recently registered device, Vasamed, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Vasamed, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Vasamed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vasamed, Inc. in the registry?
The most recently registered devices listed for Vasamed, Inc. include SENSILASE PAD-IQ.