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Luminopia

by Luminopia, Inc. United States 510(k)

510(k) K233720

Product code QQU

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK233720 Date8 Aug 2024ClearedStatusActive

Coverage

1 jurisdiction

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  • Active
  • Not covered

United States — FDA 510(k) Active

Recalls: none on record (FDA, checked 11 Oct 2026)

Specification

510(k) · synced 11 Oct 2026

510(k) Number
FDA Product Code
QQU
Device Class
Class II
Regulation
21 CFR Part 886.5500
Advisory Committee
Ophthalmic
FDA Decision
SESE Substantially Equivalent

Properties & raw data

Show properties, registry sources and raw records

Sources (1)

  • FDA 510(k) K233720 24 fields · synced 11 Oct 2026