Arx MIS

GUDID 00190837144685

Life Spine, Inc.

Spinal bone screw, non-bioabsorbable
Primary Device ID00190837144685
NIH Device Record Keya8e658e1-b203-4802-b103-24ce09456dd7
Commercial Distribution StatusIn Commercial Distribution
Brand NameArx MIS
Version Model Number12-4540-03
Company DUNS183641617
Company NameLife Spine, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100190837144685 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWPAppliance, Fixation, Spinal Interlaminal

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2026-02-19
Device Publish Date2026-02-11

On-Brand Devices [Arx MIS]

00190837171537175-045
0019083714495112-8555-03
0019083714494412-8550-03
0019083714493712-8545-03
0019083714492012-8540-03
0019083714491312-8535-03
0019083714490612-8530-03
0019083714489012-7555-03
0019083714488312-7550-03
0019083714487612-7545-03
0019083714486912-7540-03
0019083714485212-7535-03
0019083714484512-7530-03
0019083714483812-6555-03
0019083714482112-6550-03
0019083714481412-6545-03
0019083714480712-6540-03
0019083714479112-6535-03
0019083714478412-6530-03
0019083714477712-5555-03
0019083714476012-5550-03
0019083714475312-5545-03
0019083714474612-5540-03
0019083714473912-5535-03
0019083714472212-5530-03
0019083714471512-4555-03
0019083714470812-4550-03
0019083714469212-4545-03
0019083714468512-4540-03
0019083714467812-4535-03
0019083714466112-4530-03

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