Not currently registered with FDA under this name
Bio-Lok Intl., Inc.
Springfield, NJ, United States. Named as applicant on 3 dental 510(k) clearances between 2004 and 2006. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 32004–2006
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 2000–2026
510(k) clearances
Clearances on which FDA names Bio-Lok Intl., Inc. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 16 Mar 2006 | K060285 | BONEGEN - TR | LYC Synthetic Bone Grafting Material |
| 22 Oct 2004 | K041136 | MODIFICATION TO SILHOUETTE IC OR SILHOUETTE; LASER-LOK SURFACE TREATMENT -OPTIONAL SURFACE MODIFICATION TO IMPLANTS | DZE Root-Form Endosseous Implant |
| 4 Mar 2004 | K032454 | SILHOUETTE(TM) IC OR SILHOUETTE(TM) & LASER-LOK (TM) | DZE Root-Form Endosseous Implant |
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.