Home / Companies / Orion Corporation Soredex

Orion Corporation Soredex

FDA Regulatory Profile

Orion Corporation Soredex appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 30, 1998.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K983267DIGORA FOR WINDOWS 2.0December 30, 1998
K974877CRANEX TOME CEPH, OR CRANEX TOMEMarch 27, 1998
K934949DIGORAFebruary 10, 1994
K880982ORALIX PAN DC III CEPH OR PANORAMIC MODE ONLYJune 6, 1988

FDA data resources