Manufacturer registered with FDA

MuReva Phototherapy Inc.

Brecksville, OH, United States. Lists 1 dental device type with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.

FDA owner/operator10095895Specification developer1 clearance in five years

Device types listed: 1
Brands and models: 1
510(k) clearances: 12025–2025
Markets registered in: 1United States
Establishments: 1United States

510(k) clearances per year, 2007–2026

Devices listed with FDA

What MuReva Phototherapy Inc. currently lists, by FDA device type, with the brand and model names on the listing.

Device type	Category	Role	Brands and models	Listed since
Intraoral Phototherapy DeviceSGQ · Class 2	—	Maker	MuReva OM	2026

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

510(k) clearances

Clearances on which FDA names MuReva Phototherapy Inc. as the applicant.

Decided	510(k)	Device	Device type
26 Nov 2025	DEN240077	MuReva OM	SGQ Intraoral Phototherapy Device

Registered establishments

Establishment	Location	What it does
MUREVA PHOTOTHERAPY INC.FDA reg. 3045323553	Brecksville, OH, United States	Complaint file establishment, Specification developer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10095895). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.