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VATS Singley Tuttle Lung Grasping Forceps 2601-822

by Sontec Instruments, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00192896108424 UDI-DI Date5 May 2021ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
VATS Singley Tuttle Lung Grasping Forceps
Generic Name
Surgical soft-tissue manipulation forceps, scissors-like, reusable
Model / Reference
2601-822
Primary DI / UDI-DI
00192896108424
FDA Product Code
GCJ
GMDN Term
Surgical soft-tissue manipulation forceps, scissors-like, reusable
Device Class
Class II
Regulation Number
876.1500
GUDID distribution status
In Commercial Distribution
Size
Length — 13 Inch

Related devices

Category: Surgical soft-tissue manipulation forceps, scissors-like, reusable

Other devices from Sontec Instruments, Inc.

See all devices from Sontec Instruments, Inc. →

Properties

  • Prescription Use
  • Lot / Batch Number

Other properties (12)

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