Medical Device Manufacturer · FI , Helsinki

Orion Corporation Soredex - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1988

Recent clearances: DIGORA FOR WINDOWS 2.0, CRANEX TOME CEPH, OR CRANEX TOME, DIGORA

View 4 510(k) Devices ↓

4

Total

4

Cleared

0

Denied

FDA 510(k) Regulatory Record - Orion Corporation Soredex Radiology ✕

4 devices

1-4 of 4

Cleared Dec 30, 1998

DIGORA FOR WINDOWS 2.0

Radiology · 104d

Cleared Mar 27, 1998

CRANEX TOME CEPH, OR CRANEX TOME

Radiology · 88d

Cleared Feb 10, 1994

Radiology · 115d

Cleared Jun 06, 1988

ORALIX PAN DC III CEPH OR PANORAMIC MODE ONLY

Radiology · 90d