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Micasept Extraction Forceps 26934-72-004

by Sontec Instruments, Inc.

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

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 NumberB09926934720040 UDI-DI Date4 Oct 2016ListedStatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Micasept Extraction Forceps
Generic Name
Rigid endoscopic tissue manipulation forceps, reusable
Model / Reference
26934-72-004
Primary DI / UDI-DI
B09926934720040
510(k) Number
FDA Product Code
GCJ
GMDN Term
Rigid endoscopic tissue manipulation forceps, reusable
Device Class
Class II
Regulation Number
876.1500
GUDID distribution status
Not in Commercial Distribution
Size
Length — 350 Millimeter

Related devices

Cleared under the same submission (K002877)

Show all (12)

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