Optimize, Inc. is one of 26088 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Optimize, Inc. - FDA 510(k) Cleared Devices
Recent clearances: OPTIVU HDVD SYSTEM
1
Total
1
Cleared
0
Denied
Optimize, Inc. has 1 FDA 510(k) cleared medical devices. Based in Los Gatos, US.
Historical record: 1 cleared submissions from 2000 to 2000. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Optimize, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Optimize, Inc.
1 devices