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Integra® 3724030

by Integra LifeSciences Production Corporation

Integra® 3724030 is a Class I device made by Integra LifeSciences Production Corporation, listed in FDA GUDID since 24 Oct 2018 (UDI-DI 10381780082996), 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 Number10381780082996 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  • Withdrawn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
Middle ear incus hook
Model / Ref / Catalog
3724030
Primary DI / UDI-DI
10381780082996
FDA product code
JYL
GMDN term
Middle ear incus hook
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Angle — 90 degree
Outer Diameter — 1 Millimeter

Related devices

Category: Incus hook

Similar devices

Other devices filed under FDA product code JYL (HOOK, MICROSURGICAL EAR).

Other devices from Integra LifeSciences Production Corporation

See all devices from Integra LifeSciences Production Corporation →

Properties

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