Omnilight, Inc.
Country not established
- Devices
- 1
What Omnilight, Inc. makes
Omnilight, Inc. manufactures surgical and dental light sources, including the OMNILIGHT VL-2004 (surgical light), PL-2004 (periodontal light), DL-2004 (dental light), and WL-2004 (wound light). These devices are designed for illumination in clinical procedures across oral and soft-tissue applications.
The company’s products fall under FDA Class II devices and are recorded in the 510(k) clearance registry. Omnilight, Inc. is headquartered in the United States.
Catalogue
Omnilight Vl-2004, Pl-2004, Dl-2004, And Wl-2004 Ref K040664
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Omnilight, Inc. have in the registry?
The registry currently lists 1 device for Omnilight, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Omnilight, Inc.'s devices?
Among its 1 most recently registered device, Omnilight, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Omnilight, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Omnilight, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Omnilight, Inc. in the registry?
The most recently registered devices listed for Omnilight, Inc. include OMNILIGHT VL-2004, PL-2004, DL-2004, AND WL-2004.