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RetinaLogik rvf200

by Retinalogik Inc.

RetinaLogik rvf200 is a Class I device made by Retinalogik Inc., listed in FDA GUDID since 7 Mar 2025 (UDI-DI G617RVF2001), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberG617RVF2001 UDI-DI Date7 Mar 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  • Withdrawn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
RetinaLogik
Generic name
Perimeter, automatic
Model / reference
rvf200
Primary DI / UDI-DI
G617RVF2001
FDA product code
HPT
GMDN term
Perimeter, automatic
Device class
Class I
Regulation number
886.1605
GUDID distribution status
In Commercial Distribution

Related devices

Category: Perimeter, automatic

Similar devices in this category

Other devices filed under Perimeter, automatic.

Other devices from Retinalogik Inc.

Properties

  • Prescription use
  • Premarket exempt
Other properties (13, all answered No)