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EndoVue 90K0089

by Nds Surgical Imaging, LLC.

EndoVue 90K0089 is a Class I device made by Nds Surgical Imaging, LLC., listed in FDA GUDID since 24 Jun 2022 (UDI-DI 00851455007966), 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 Number00851455007966 UDI-DI Date24 Jun 2022ListedStatusListed 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  • Withdrawn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
EndoVue
Generic name
Image display unit, colour
Model / reference
90K0089
Primary DI / UDI-DI
00851455007966
FDA product code
KQM
GMDN term
Image display unit, colour
Device class
Class I
Regulation number
878.4160
GUDID distribution status
In Commercial Distribution

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Category: Image display unit, colour

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Properties

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