Not currently registered with FDA under this name
Belport Company, Inc., Gingi-Pak
Camarillo, CA, United States. Named as applicant on 7 dental 510(k) clearances between 2020 and 2026. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 72020–2026
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 2007–2026
510(k) clearances
Clearances on which FDA names Belport Company, Inc., Gingi-Pak as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 10 Apr 2026 | K260430 | Porcelain Etch Gel | KLE Resin Tooth Bonding Agent |
| 2 Sep 2025 | K251775 | RODIN Cement | EMA Dental Cement |
| 7 May 2025 | K250222 | SDF Pro | PHR Diammine Silver Fluoride Dental Hypersensitivity Varnish |
| 20 Jun 2024 | K240688 | RODIN Titan 3D Resin | EBI Rebasing Repairing Relining Denture Resin |
| 13 Jun 2024 | K231060 | ProMin Dental Desensitizing Gel | LBH Cavity Varnish |
| 27 Mar 2023 | K223365 | RODIN Palette Naturalizing Kit | EBD Resin Filling Material Coating |
| 2 Sep 2020 | K200462 | EtchPro Etching Gel | KLE Resin Tooth Bonding Agent |
Some of these clearances are listed with FDA today by another company: Pac-Dent Inc. (5), The Belport Company, Inc. DBA Gingi-Pak (2), Hiossen Inc. (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.