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CUSA® Excel C2602

by Integra Lifesciences (Ireland) Limited

CUSA® Excel C2602 is a device classified as Unclassified made by Integra Lifesciences (Ireland) Limited, listed in FDA GUDID since 29 Dec 2016 (UDI-DI 10381780039433), 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 Number10381780039433 UDI-DI Date29 Dec 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  • Withdrawn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
CUSA® Excel
Generic name
Soft-tissue ultrasonic surgical system handpiece, reusable
Model / Ref / Catalog
C2602
Primary DI / UDI-DI
10381780039433
FDA product code
LFL, LBK
GMDN term
Soft-tissue ultrasonic surgical system handpiece, reusable
Device class
U
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code LFL (Instrument, ultrasonic surgical).

Other devices from Integra Lifesciences (Ireland) Limited

See all devices from Integra Lifesciences (Ireland) Limited →

Properties

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