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Visionix Retinomax 5

by Right Mfg. Co., Ltd. 3 variants

Visionix Retinomax 5 (VSN5100TB) is a Class I device made by Right Mfg. Co., Ltd., listed in FDA GUDID since 5 Jan 2023 (UDI-DI 04580606431652), 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 Number04580606431652 UDI-DI Date5 Jan 2023ListedStatusListed 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  • Withdrawn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
Visionix
Generic name
Automated ophthalmic refractometer
Model / Ref / Catalog
Retinomax 5, VSN5100TB
Primary DI / UDI-DI
04580606431652
FDA product code
HKO
GMDN term
Automated ophthalmic refractometer
Device class
Class I
Regulation number
886.1760
GUDID distribution status
In Commercial Distribution

Related devices

Category: Automated ophthalmic refractometer

Similar devices in this category

Other devices filed under Automated ophthalmic refractometer.

Other devices from Right Mfg. Co., Ltd.

See all devices from Right Mfg. Co., Ltd. →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)