Medical Device Manufacturer · FI , Tuusula

Instrumentarium Dental, Palodex Group OY - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2007

Total

Cleared

Denied

Instrumentarium Dental, Palodex Group OY has 5 FDA 510(k) cleared medical devices. Based in Tuusula, FI.

Historical record: 5 cleared submissions from 2007 to 2014. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Instrumentarium Dental, Palodex Group OY Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Instrumentarium Dental, Palodex Group OY

5 devices

1-5 of 5