UDI device identifier
IdentiTi 121-07092220
UDI device identifier 00190376220482 · ALPHATEC SPINE, INC.
Key facts
| Primary DI | 00190376220482 |
|---|---|
| Brand name | IdentiTi |
| Version or model | 121-07092220 |
| Company | ALPHATEC SPINE, INC. |
| DUNS number | 602465783 |
| Product code | MAX |
| GMDN term | Spinal implant trial |
| Premarket submission | K241375 |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jan 21, 2026 |
| Version date | Jan 29, 2026 |
| Description | IDENTITi PS POROUS Ti TRIAL, 7 X 9 X 22 mm, 20° |
At a glance
- None MAUDE reports citing this UDI
- Yes 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: