Ortho-Pro, LLC

FDA Regulatory Profile

Ortho-Pro, LLC 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 January 14, 2011.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K102601ORTHOFLEX RODJanuary 14, 2011
K094037TC PLATING SYSTEMMarch 10, 2010
K042310ORTHO-PRO CANNULATED BONE SCREWSSeptember 16, 2004
K032682STS SCREWOctober 22, 2003