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symphonX™ Hook-knife

by Fortimedix Surgical B.V. GUDID

Listed FDA GUDID listing, not in commercial distribution

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08719324463157 UDI-DIDate15 Feb 2017ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
symphonX™
Generic Name
Endoscopic electrosurgical electrode, monopolar, single-use
Model / Ref / Catalog
Hook-knife, 314-005
Primary DI / UDI-DI
08719324463157
FDA Product Code
GCJ
GMDN Term
Endoscopic electrosurgical electrode, monopolar, single-use
Device Class
Class II
Regulation Number
876.1500
GUDID distribution status
Not in Commercial Distribution

Other devices from Fortimedix Surgical B.V.

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No