Pontemedag - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Pontemedag has 1 FDA 510(k) cleared medical devices. Based in Arbon, CH.
Latest FDA clearance: Apr 2026. Active since 2026. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Pontemedag Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hyman, Phelps & McNamara, P.C. as regulatory consultant.
1 devices