Medical Device Manufacturer · US , Miami , FL

Syntheon, LLC - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2008

Total

Cleared

Denied

Syntheon, LLC has 2 FDA 510(k) cleared medical devices. Based in Miami, US.

Latest FDA clearance: Aug 2023. Active since 2008. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Syntheon, LLC Filter by specialty or product code using the sidebar.

2 devices

1–2 of 2