UDI device identifier
8 Degree Lordotic, Opticage Expandable Interbody Implant 9101-21
UDI device identifier 00011954013448 · INTERVENTIONAL SPINE, INC
Key facts
| Primary DI | 00011954013448 |
|---|---|
| Brand name | 8 Degree Lordotic, Opticage Expandable Interbody Implant |
| Version or model | 9101-21 |
| Catalog number | 9101-21 |
| Company | INTERVENTIONAL SPINE, INC |
| DUNS number | 017663522 |
| Product code | MAX |
| GMDN term | Metallic spinal interbody fusion cage |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | Yes |
| Publish date | May 25, 2016 |
| Version date | Jul 14, 2025 |
| Description | 22mm Width x 45mm Length by 11mm-16mm Footprint Length |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 1,000+ GUDID devices with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About UDI device identifiers (GUDID)
The Global Unique Device Identification Database (GUDID) holds the device identifiers (UDI-DIs) and key attributes that labelers submit to the FDA for devices that carry a unique device identifier.
Source: U.S. FDA Global Unique Device Identification Database (GUDID), via NLM AccessGUDID · Source date: