Prodrive Systems, Inc. is one of 648 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Prodrive Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PRODRIVE LINE OF DENTAL HANDPIECES, DO-ALL DENTAL HANDPIECE LUBRICANT, PRODRIVE SYSTEMS REPLACEMENT TURBINE
3
Total
3
Cleared
0
Denied
Prodrive Systems, Inc. has 3 FDA 510(k) cleared medical devices. Based in Spencerville, Ontario, CA.
Historical record: 3 cleared submissions from 2006 to 2009. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Prodrive Systems, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Prodrive Systems, Inc.
3 devices