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ClosureFast Tumescent Infiltration Kit TIK-01

by Argon Medical Devices, Inc. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00886333227570 UDI-DIDate29 Jul 2024ListedStatusListed GUDID: 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  • Withdrawn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 22 Oct 2026.

Specification

GUDID

Trade Name
ClosureFast Tumescent Infiltration Kit
Generic Name
General surgical procedure kit, non-medicated, reusable
Model / Ref / Catalog
TIK-01
Primary DI / UDI-DI
00886333227570
FDA Product Code
OEQ
GMDN Term
General surgical procedure kit, non-medicated, reusable
Device Class
Class II
Regulation Number
870.1650
GUDID distribution status
In Commercial Distribution

Related devices

Category: General surgical procedure kit, non-medicated, reusable

Other devices from Argon Medical Devices, Inc.

See all devices from Argon Medical Devices, Inc. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Convenience Kit
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (6)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No