Lighted Magnetic Foreign Body Removal Tool 3525

GUDID 10714646001532

Lighted Magnetic Foreign Body Remover - 5ct

Bionix, LLC

Abdominal/ENT/orthopaedic surgical probe, single-use
Primary Device ID10714646001532
NIH Device Record Keydfe0993c-226b-4590-8059-f51871b03097
Commercial Distribution StatusIn Commercial Distribution
Brand NameLighted Magnetic Foreign Body Removal Tool
Version Model Number3525
Catalog Number3525
Company DUNS117844489
Company NameBionix, LLC
Device Count5
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)551-7096
EmailBionix@bionix.com
Phone+1(800)551-7096
EmailBionix@bionix.com
Phone+1(800)551-7096
EmailBionix@bionix.com
Phone+1(800)551-7096
EmailBionix@bionix.com
Phone+1(800)551-7096
EmailBionix@bionix.com
Phone+1(800)551-7096
EmailBionix@bionix.com
Phone+1(800)551-7096
EmailBionix@bionix.com
Phone+1(800)551-7096
EmailBionix@bionix.com
Phone+1(800)551-7096
EmailBionix@bionix.com
Phone+1(800)551-7096
EmailBionix@bionix.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100714646001535 [Primary]
GS110714646001532 [Unit of Use]

FDA Product Code

KAKPROBE, ENT

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2026-03-11
Device Publish Date2026-03-03

On-Brand Devices [Lighted Magnetic Foreign Body Removal Tool]

00714646001627Lighted Magnetic Foreign Body Remover - 1ct
10714646001532Lighted Magnetic Foreign Body Remover - 5ct

© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.