The Belport Company Inc., DBA Gingi-Pak is one of 12913 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Belport Company Inc., DBA Gingi-Pak - FDA 510(k) Cleared Devices
Recent clearances: PacTemp Automix NE
1
Total
1
Cleared
0
Denied
The Belport Company Inc., DBA Gingi-Pak has 1 FDA 510(k) cleared medical devices. Based in Camarillo, US.
Latest FDA clearance: Aug 2026. Active since 2026. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by The Belport Company Inc., DBA Gingi-Pak Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - The Belport Company Inc., DBA Gingi-Pak
1 devices