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Gynex 2781

by Gynex Corporation

Gynex 2781 is a vaginal speculum (FDA Class I; FDA product code HDF, Speculum, Vaginal, Metal) made by Gynex Corporation, listed in FDA GUDID since 12 Dec 2023 (UDI-DI GYNX27810), 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 NumberGYNX27810 UDI-DI Date12 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  • Withdrawn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
Vaginal speculum, reusable
Model / reference
2781
Primary DI / UDI-DI
GYNX27810
FDA product code
HDF
GMDN term
Vaginal speculum, reusable
Device class
Class I
Regulation number
884.4520
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Vaginal speculum, reusable

Similar devices

Other devices filed under FDA product code HDF (Speculum, Vaginal, Metal).

Other devices from Gynex Corporation

See all devices from Gynex Corporation →

Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)