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Disposable Biopsy Forceps Fb-221D

by Olympus Medical Systems Corporation GUDID 3 variants

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04953170467608 UDI-DIDate9 Apr 2026ListedStatusListed 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  • Withdrawn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
Disposable Biopsy Forceps
Generic Name
Flexible endoscopic biopsy forceps, single-use
Model / Ref / Catalog
FB-221D, N5431942
Primary DI / UDI-DI
04953170467608
510(k) Number
FDA Product Code
EOB, EOQ
GMDN Term
Flexible endoscopic biopsy forceps, single-use
Device Class
Class II
Regulation Number
874.4760, 874.4680
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K250957)

Cleared under the same submission (K252050)

Other devices from Olympus Medical Systems Corporation

See all devices from Olympus Medical Systems Corporation →

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