FDA UDI In Commercial Distribution 🇺🇸 United States

Px®

DI: M711LS26480 · Model: LS-264-8 · 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
M711LS26480
Version / Model
LS-264-8
Catalog Number
LS-264-8
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
5
Public Version Date
2026-01-09
Public Version Status
Update
Public Device Record Key
ea45e23e-d3a4-4b0c-9ce9-d66955ee503e

Device Description

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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Primary M711LS26480

Customer Contacts

Phone
801-261-2236

Device Sizes

Type Value Unit Text
Height 8 Millimeter
Width 10 Millimeter