Medical Device Manufacturer · US , Stamford , CT

Orthocon, Inc. - FDA 510(k) Cleared Devices

34 submissions · 34 cleared · Since 2006
34
Total
34
Cleared
0
Denied

Orthocon, Inc. has 34 FDA 510(k) cleared medical devices. Based in Stamford, US.

Latest FDA clearance: Mar 2026. Active since 2006. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Orthocon, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Mcra, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Orthocon, Inc.
34 devices
1-12 of 34
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