Skip to content

Auto Refkeratometer Rc-5000

by Tomey Corporation 2 variants

Auto Refkeratometer Rc-5000 is a Class I device made by Tomey Corporation, listed in FDA GUDID since 30 Oct 2020 (UDI-DI 04582273612242), 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 Number04582273612242 UDI-DI Date30 Oct 2020ListedStatusListed 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  • Withdrawn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
Auto Refkeratometer
Generic name
Automated ophthalmic refractometer
Model / reference
RC-5000
Primary DI / UDI-DI
04582273612242
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 Tomey Corporation

See all devices from Tomey Corporation →

Properties

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