Not currently registered with FDA under this name
Biomet Interpore Cross
Irvine, CA, United States. Named as applicant on 1 dental 510(k) clearance between 2012 and 2012. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 12012–2012
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 2007–2026
510(k) clearances
Clearances on which FDA names Biomet Interpore Cross as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 20 Jan 2012 | K113645 | REGENEROSS ALLOGRAFT PLUS MINERLIZED | NUN Human Source Bone Grafting Material |
Some of these clearances are listed with FDA today by another company: ZimVie US Corp LLC (1).
Sources
FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.