FDA UDI In Commercial Distribution 🇺🇸 United States

Arx MIS

DI: 00190837170943 · Model: 14602-110 · Life Spine, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Arx MIS
Primary DI
00190837170943
Version / Model
14602-110
Company Name
Life Spine, Inc.
Labeler DUNS
183641617
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-02-13
Public Version
1
Public Version Date
2026-02-23
Public Version Status
New
Public Device Record Key
c5a93265-980b-4128-bd72-dfb0e7b57c3d

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KWP Appliance, Fixation, Spinal Interlaminal
NKB Thoracolumbosacral Pedicle Screw System

GMDN Terms

Code Name
65116 Bone-screw internal spinal fixation system rod

Identifiers

Type ID
Primary 00190837170943

Premarket Submissions

Submission Number Supplement Number
K233455 000