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EyeCaster BSI-14-HS-BQ900

by Innovations Lightx Inc

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860012447121 UDI-DI Date12 Nov 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
EyeCaster
Generic Name
Smartphone camera ophthalmic imaging lens
Model / Reference
BSI-14-HS-BQ900
Primary DI / UDI-DI
00860012447121
FDA Product Code
PJZ
GMDN Term
Smartphone camera ophthalmic imaging lens
Device Class
Class II
Regulation Number
886.1120
GUDID distribution status
In Commercial Distribution

Other devices from Innovations Lightx Inc

Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Serial Number
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Expiration Date: No