Mureva Phototherapy, Inc.
United Statesfrom the FDA registration address FDA FEI 3045323553
- Devices
- 5
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Mureva Phototherapy, Inc. makes
Mureva Phototherapy, Inc. manufactures the MuReva OM™, a phototherapy device designed for medical use in specific clinical applications requiring controlled light exposure.
The company’s portfolio is regulated under FDA’s Class II device classification, with the MuReva OM™ authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
MuReva OM™ Ref DEN240077
Regimes: De Novo Registry: De Novo
Company details
- FDA FEI number
- 3045323553
- DUNS number
- 117861215
- Address
- 6611 W Snowville Rd, Brecksville, OH, 44141
Frequently asked questions
How many devices does Mureva Phototherapy, Inc. have in the registry?
The registry currently lists 5 devices for Mureva Phototherapy, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mureva Phototherapy, Inc.'s devices?
Among its 5 most recently registered devices, Mureva Phototherapy, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (4 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Mureva Phototherapy, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Mureva Phototherapy, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mureva Phototherapy, Inc. in the registry?
The most recently registered devices listed for Mureva Phototherapy, Inc. include MuReva OM™ 1000155, MuReva OM™ 1000300, MuReva OM™ 1000329 and MuReva OM™ 1000307.