Oroscience, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Oroscience, Inc. makes
Oroscience, Inc. manufactures the Curative980 Diode Laser, a medical laser device designed for soft tissue procedures, and PerioGenix, a periodontal treatment solution intended for gum disease management.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance. Both devices are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
CURATIVE980 Diode Laser Ref K082445
Regimes: 510(k) Registry: 510(k)Periogenix Ref K083516
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Oroscience, Inc. have in the registry?
The registry currently lists 2 devices for Oroscience, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oroscience, Inc.'s devices?
Among its 2 most recently registered devices, Oroscience, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Oroscience, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Oroscience, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oroscience, Inc. in the registry?
The most recently registered devices listed for Oroscience, Inc. include CURATIVE980 DIODE LASER and PERIOGENIX.