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Integra® 1422100

by Integra LifeSciences Production Corporation

Integra® 1422100 is a Class I device made by Integra LifeSciences Production Corporation, listed in FDA GUDID since 16 Apr 2018 (UDI-DI 10381780074915), 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 Number10381780074915 UDI-DI Date16 Apr 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  • Withdrawn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
Laryngeal knife
Model / Ref / Catalog
1422100
Primary DI / UDI-DI
10381780074915
FDA product code
JZY
GMDN term
Laryngeal knife
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution

Related devices

Category: Laryngeal knife

Similar devices in this category

Other devices filed under Laryngeal knife.

Other devices from Integra LifeSciences Production Corporation

See all devices from Integra LifeSciences Production Corporation →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)