Cell Robotics, Inc.
United StatesFDA applicant, unverified
- Devices
- 9
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Lasette Ref K983673
Regimes: 510(k) Registry: 510(k)Cell Robotics' Lasette Ref K981746
Regimes: 510(k) Registry: 510(k)Clinical Lasette P-200 Ref K033799
Regimes: 510(k) Registry: 510(k)Cell Robotics Er: Yag Surgical Laser Ref K970461
Regimes: 510(k) Registry: 510(k)Cell Robotics Ultra-Light Peel Laser System Ref K021946
Regimes: 510(k) Registry: 510(k)Lasette Laser Skin Perforator Ref K982230
Regimes: 510(k) Registry: 510(k)Lasette Laser Skin Perforator Ref K981149
Regimes: 510(k) Registry: 510(k)Lasette Ref K973431
Regimes: 510(k) Registry: 510(k)Lasette Ref K965124
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cell Robotics, Inc. have in the registry?
The registry currently lists 9 devices for Cell Robotics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cell Robotics, Inc.'s devices?
Among its 9 most recently registered devices, Cell Robotics, Inc. has devices listed in FDA 510(k) (9 devices).
What risk classes do Cell Robotics, Inc.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for Cell Robotics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cell Robotics, Inc. in the registry?
The most recently registered devices listed for Cell Robotics, Inc. include LASETTE, CELL ROBOTICS' LASETTE, CLINICAL LASETTE P-200 and CELL ROBOTICS ER: YAG SURGICAL LASER.