FDA UDI In Commercial Distribution 🇺🇸 United States

Tx™

DI: M711LS3960 · Model: LS-396 · INNO Holdings, Inc.
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Tx™
Primary DI
M711LS3960
Version / Model
LS-396
Company Name
INNO Holdings, Inc.
Labeler DUNS
141620464
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-03-31
Public Version
4
Public Version Date
2026-01-15
Public Version Status
Update
Public Device Record Key
7bd9a6ad-4eea-4409-adaa-3d871db649e2

Device Description

SST, Silicone, PEEK

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
No
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
12696 Orthopaedic inorganic implant inserter/extractor, reusable
32865 Orthopaedic implant driver

Identifiers

Type ID
Primary M711LS3960

Customer Contacts

Phone
801-261-2236