Medical Device Manufacturer · US , Ormond Beach , FL

Citieffe - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2012

Total

Cleared

Denied

Citieffe has 3 FDA 510(k) cleared medical devices. Based in Ormond Beach, US.

Historical record: 3 cleared submissions from 2012 to 2012. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Citieffe

3 devices

1-3 of 3