# Belport Company, Inc., Gingi-Pak

- Location (FDA's records): Camarillo, CA
- FDA decisions: 11 (2020–2026): 11 510(k) clearances
- Product codes: MVL (2), KLE (2), EBI (1), PHR (1), EMA (1), MQC (1), LBH (1), KJJ (1), EBD (1)
- 510(k) review time since 2016: median 145 days, against 151 for FDA's reviews in the same codes and years (3 of 6 faster)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Inter-Med/Vista Dental Products: 2 (https://510kreport.com/company/inter-med-vista-dental-products)
- Sprintray, Inc.: 1 (https://510kreport.com/company/sprintray)
- Pac-Dent, Inc.: 1 (https://510kreport.com/company/pac-dent)
- Pulpdent Corp.: 1 (https://510kreport.com/company/pulpdent)

## Firms that cite its devices most
- 3BFAB Teknoloji a.S.: 1 (https://510kreport.com/company/3bfab-teknoloji)

## Its most-cited devices
- K240688: RODIN Titan 3D Resin (2024), cited by 1

## Recent decisions
- K260430: Porcelain Etch Gel (Apr 10, 2026)
- K251775: RODIN Cement (Sep 2, 2025)
- K250279: RC-SwiftPrep (Jul 2, 2025)
- K250222: SDF Pro (May 7, 2025)
- K240688: RODIN Titan 3D Resin (Jun 20, 2024)
- K231060: ProMin Dental Desensitizing Gel (Jun 13, 2024)
- K231793: RODIN 3D Resin SPLINT, Hard/Flex (Mar 26, 2024)
- K223365: RODIN Palette Naturalizing Kit (Mar 27, 2023)

Source page: https://510kreport.com/company/belport-company-gingi-pak