FDA UDI In Commercial Distribution 🇺🇸 United States

Px®

DI: M711LS2580 · Model: LS-258 · INNO Holdings, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Px®
Primary DI
M711LS2580
Version / Model
LS-258
Catalog Number
LS-258
Company Name
INNO Holdings, Inc.
Labeler DUNS
141620464
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-13
Public Version
4
Public Version Date
2026-01-08
Public Version Status
Update
Public Device Record Key
cebfd331-3abb-4e07-aacc-127fbe38993f

Device Description

Silicone, SST

Device Characteristics

Single Use
No
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
Yes
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
32865 Orthopaedic implant driver

Identifiers

Type ID
Primary M711LS2580

Customer Contacts

Phone
801-261-2236