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Enteroscope Vsb-2990I

by PENTAX of America Inc.

Enteroscope Vsb-2990I is a Class II device made by PENTAX of America Inc., listed in FDA GUDID since 13 Mar 2018 (UDI-DI 04961333240470), registry data as of 8 Nov 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04961333240470 UDI-DI Date13 Mar 2018ListedStatusListed 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  • Withdrawn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
Enteroscope
Generic name
Flexible video enteroscope
Model / reference
VSB-2990I
Primary DI / UDI-DI
04961333240470
FDA product code
FDS
GMDN term
Flexible video enteroscope
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Flexible video enteroscope

Similar devices

Other devices filed under FDA product code FDS (Gastroscope And Accessories, Flexible/Rigid).

Other devices from PENTAX of America Inc.

See all devices from PENTAX of America Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)