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Manifold Vision Meter 001.000.005 (with TÜV SÜD safety mark)

by Adaptive Sensory Technology 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 Number00850067216025 UDI-DI Date21 May 2026ListedStatusListed 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  • Withdrawn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
Manifold Vision Meter
Generic Name
Visual acuity projector
Model / Reference
001.000.005 (with TÜV SÜD safety mark)
Primary DI / UDI-DI
00850067216025
FDA Product Code
QTO
GMDN Term
Visual acuity projector
Device Class
Class I
Regulation Number
886.1150
GUDID distribution status
In Commercial Distribution

Other devices from Adaptive Sensory Technology Inc

Properties

  • Premarket Exempt
  • Serial Number

Other properties (12)

  • 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
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No