Orthocor Medical is one of 22227 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Orthocor Medical - FDA 510(k) Cleared Devices
Recent clearances: ORTHOCOR ACTIVE DEVICE ORTHOCOR GENERAL USE ACTIVE DEVICE, ORTHOCOR KNEE SYSTEM, MEDIAN, LARGE, X-LARGE, ORTHOCOR KNEE SYSTEM BASIC
3
Total
3
Cleared
0
Denied
Orthocor Medical, develops wearable, noninvasive pain management devices using Pulsed Shortwave Therapy (PST) technology. The company specializes in drug-free solutions for post-operative, acute, arthritic, and chronic pain relief across multiple body areas.
Orthocor Medical has received 3 FDA 510(k) clearances from 3 total submissions in the Physical Medicine device category. The company's regulatory history spans from 2009 to 2013. As a historical record, Orthocor Medical has not received clearances in more than five years and is no longer actively submitting devices to the FDA.
The company's cleared devices include active therapeutic systems designed for knee and multi-body applications, as well as general-use active devices for physical medicine. Products feature wearable form factors enabling patient mobility during treatment.
Explore the company's complete FDA 510(k) clearance history, device names, product codes, and clearance dates in the database.
FDA 510(k) Regulatory Record - Orthocor Medical
3 devices