Nanospectra Biosciences, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
AuroLase® System Ref K243701
Regimes: 510(k) Registry: 510(k)Aurolase Therapy, Laser Delivery Device (LDD) Ref K202953
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nanospectra Biosciences, Inc. have in the registry?
The registry currently lists 2 devices for Nanospectra Biosciences, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nanospectra Biosciences, Inc.'s devices?
Among its 2 most recently registered devices, Nanospectra Biosciences, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Nanospectra Biosciences, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Nanospectra Biosciences, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nanospectra Biosciences, Inc. in the registry?
The most recently registered devices listed for Nanospectra Biosciences, Inc. include AuroLase® System and Aurolase Therapy, Laser Delivery Device (LDD).