Skip to content

Diamond Sight CS-8812

by Wave Optiks Eyewear 2 variants

Diamond Sight CS-8812 is a Class I device made by Wave Optiks Eyewear, listed in FDA GUDID since 20 Sep 2022 (UDI-DI 00810000183876), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810000183876 UDI-DI Date20 Sep 2022ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Diamond Sight
Generic name
Non-prescription sunglasses
Model / reference
CS-8812
Primary DI / UDI-DI
00810000183876
FDA product code
HQY
GMDN term
Non-prescription sunglasses
Device class
Class I
Regulation number
886.5850
GUDID distribution status
In Commercial Distribution

Related devices

Category: Tinted non-prescription spectacles

Other devices from Wave Optiks Eyewear

See all devices from Wave Optiks Eyewear →

Properties

  • Over-the-counter
  • Premarket exempt
Other properties (13, all answered No)