Opusmed, Inc.
Country not established
- Devices
- 1
What Opusmed, Inc. makes
Opusmed, Inc. manufactures the LUMIPHASE-R, a medical device designed for photodynamic therapy applications, utilizing light-based treatment to target specific tissues or lesions.
The company’s portfolio is regulated under Class II devices in the United States, with the LUMIPHASE-R authorised through the FDA’s 510(k) clearance process. The manufacturer is based in the US.
Catalogue
Lumiphase-R Ref K051255
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Opusmed, Inc. have in the registry?
The registry currently lists 1 device for Opusmed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Opusmed, Inc.'s devices?
Among its 1 most recently registered device, Opusmed, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Opusmed, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Opusmed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Opusmed, Inc. in the registry?
The most recently registered devices listed for Opusmed, Inc. include LUMIPHASE-R.