Pontemedag is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Pontemedag - FDA 510(k) Cleared Devices
Recent clearances: PELVIPOWER Pelvic Functional Magnetic Stimulation (PELVIPOWER PelvicFMS) (033-0-1100-02)
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.
FDA 510(k) Regulatory Record - Pontemedag
1 devices