Rebotix - FDA 510(k) Cleared Devices

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.

510(k) submissions have been managed by Ajw Technology Consultants, Inc. as regulatory consultant.