Skip to content

Pentax Fg-29V

by Hoya Corporation

Pentax Fg-29V is a Class II device made by Hoya Corporation, listed in FDA GUDID since 7 Apr 2017 (UDI-DI 04961333228584), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04961333228584 UDI-DI Date7 Apr 2017ListedStatusListed 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  • Withdrawn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
Pentax
Generic name
Flexible fibreoptic gastroscope
Model / reference
FG-29V
Primary DI / UDI-DI
04961333228584
FDA product code
FDS
GMDN term
Flexible fibreoptic gastroscope
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code FDS (Gastroscope and accessories, flexible/rigid).

Other devices from Hoya Corporation

See all devices from Hoya Corporation →

Properties

  • Sterilise before use
  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)