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Lighted Magnetic Foreign Body Removal Tool 3525

by Bionix, LLC

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00714646001535 UDI-DI Date3 Mar 2026ListedStatusListed 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  • Withdrawn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
Lighted Magnetic Foreign Body Removal Tool
Generic Name
Abdominal/ENT/orthopaedic surgical probe, single-use
Model / Ref / Catalog
3525
Description
Lighted Magnetic Foreign Body Remover - 5ct
Primary DI / UDI-DI
00714646001535
FDA Product Code
KAK
GMDN Term
Abdominal/ENT/orthopaedic surgical probe, single-use
Device Class
Class I
Regulation Number
874.4420
GUDID distribution status
In Commercial Distribution

Other devices from Bionix, LLC

See all devices from Bionix, LLC →

Properties

  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (9)

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