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Gynex 530VCDA-R

by Gynex Corporation

Gynex 530VCDA-R is a colposcope (FDA Class II; FDA product code HEX, Colposcope (And Colpomicroscope)) made by Gynex Corporation, listed in FDA GUDID since 19 Dec 2023 (UDI-DI GYNX530VCDAR0), 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 NumberGYNX530VCDAR0 UDI-DI Date19 Dec 2023ListedStatusListed 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  • Withdrawn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
Gynex
Generic name
Colposcope
Model / reference
530VCDA-R
Primary DI / UDI-DI
GYNX530VCDAR0
FDA product code
HEX
GMDN term
Colposcope
Device class
Class II
Regulation number
884.1630
GUDID distribution status
In Commercial Distribution

Related devices

Category: Colposcope

Similar devices

Other devices filed under FDA product code HEX (Colposcope (And Colpomicroscope)).

Other devices from Gynex Corporation

See all devices from Gynex Corporation →

Properties

  • Lot / batch number
Other properties (14, all answered No)