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Flex Eyewear Frames

by Flex Eyewear, Inc.

510(k) K895371

Flex Eyewear Frames is a Class I device made by Flex Eyewear, Inc., cleared under FDA 510(k) K895371 on 21 Sep 1989, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK895371 Date21 Sep 1989ClearedStatusActive

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
HQZ
Device class
Class I
Regulation
21 CFR Part 886.5842
Advisory committee
Ophthalmic
FDA decision
SESE Substantially Equivalent

Similar devices

Other devices filed under FDA product code HQZ (Frame, Spectacle).