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Integra® 3724017

by Integra LifeSciences Production Corporation

Integra® 3724017 is a Class I device made by Integra LifeSciences Production Corporation, listed in FDA GUDID since 24 Oct 2018 (UDI-DI 10381780082880), 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 Number10381780082880 UDI-DI Date24 Oct 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  • Withdrawn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
Integra®
Generic name
Endaural surgical curette, reusable
Model / Ref / Catalog
3724017
Primary DI / UDI-DI
10381780082880
FDA product code
JYG
GMDN term
Endaural surgical curette, reusable
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Outer Diameter — 1.5 Millimeter

Related devices

Category: Endaural surgical curette, reusable

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Other devices filed under Endaural surgical curette, reusable.

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)