LUMINOPIA INC

FDA Device Registration & Listing · Cambridge, MA, US · Registration 3023855046

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3023855046
FEI Number
3023855046
Entity Name
LUMINOPIA INC
City/State/Country
Cambridge, MA, US
Establishment Address
955 Massachusetts Ave, #335, Cambridge, MA 02139, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Luminopia Inc (Owner Number: 10085892)
Owner / Operator Contact Address
955 Massachusetts Ave, #335, Cambridge, MA 02139, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
DEN210005
PMA Number
N/A

All Registered Proprietary Names

Luminopia Luminopia One

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QQU Digital Therapy Device For Amblyopia Ophthalmic Class 2 886.5500 2022-08-31

Official Correspondent

Scott Xiao

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Luminopia Inc
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3023855046. Last updated year: 2026. Please use registration number 3023855046 when referencing this establishment in official correspondence.
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