FDA UDI In Commercial Distribution 🇺🇸 United States

OptiMesh Multiplanar Expandable Interbody Fusion System

DI: M7401001341 · Model: 102-69-01 · SPINEOLOGY INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OptiMesh Multiplanar Expandable Interbody Fusion System
Primary DI
M7401001341
Version / Model
102-69-01
Catalog Number
100-1341
Company Name
SPINEOLOGY INC.
Labeler DUNS
033014361
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-07-03
Public Version
1
Public Version Date
2025-07-11
Public Version Status
New
Public Device Record Key
03e8722e-4b46-40a3-9af3-fc8aa9115ee8

Device Description

Bevel Graft Tube

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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
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
47872 Bone graft funnel

Identifiers

Type ID
Primary M7401001341

Customer Contacts

Phone
651-256-8500