Medical Device Manufacturer · US , St. Petersburg , FL

Rebotix - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2024

Total

Cleared

Denied

Rebotix has 5 FDA 510(k) cleared medical devices. Based in St. Petersburg, US.

Latest FDA clearance: Aug 2025. Active since 2024. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) cleared devices by Rebotix

5 devices

1-5 of 5