Data / Medical devices / United States / Mureva Phototherapy Inc.
Mureva Phototherapy Inc.: FDA-registered device maker in Brecksville, OH, United States, 1 510(k) clearance
Mureva Phototherapy Inc. is registered with the FDA (registration 3045323553) in Brecksville, OH, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 26, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3045323553
- Address
- 6611 W Snowville Rd, Brecksville, OH, United States, 44141
- Owner or operator
- MuReva Phototherapy Inc. (10095895)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- May 18, 2026
- Registered through
- 2026
- Brand names listed
- MuReva OM
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Intraoral Phototherapy Device | SGQ | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 26, 2025 | DEN240077 | MuReva OM | SGQ | Unknown | Mureva Phototherapy, Inc. | accessdata.fda.gov |
Updated November 26, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.