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Integra® 90520DUS

by Integra LifeSciences Production Corporation

Integra® 90520DUS is a Class II device made by Integra LifeSciences Production Corporation, listed in FDA GUDID since 31 Aug 2016 (UDI-DI 10381780168553), 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 Number10381780168553 UDI-DI Date31 Aug 2016ListedStatusListed 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  • Withdrawn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
Integra®
Generic name
General-purpose light source
Model / Ref / Catalog
90520DUS
Primary DI / UDI-DI
10381780168553
FDA product code
FSR
GMDN term
General-purpose light source
Device class
Class II
Regulation number
886.4335
GUDID distribution status
In Commercial Distribution

Related devices

Category: General-purpose light source

Similar devices

Other devices filed under FDA product code FSR (Light, headband, surgical).

Other devices from Integra LifeSciences Production Corporation

See all devices from Integra LifeSciences Production Corporation →

Properties

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