Tigon Medical - FDA 510(k) Cleared Devices

Tigon Medical, designs and sells surgical implants, instruments, and suture for the sports medicine industry. Founded in 2017, the company is focused on delivering innovative suture anchors while minimizing waste in surgical procedures. The company operates with a manufacturing facility in Severna Park, Maryland.

Tigon Medical has received 7 FDA 510(k) clearances from 7 total submissions, with all submissions focused on Orthopedic devices. The company's regulatory track record spans from 2019 to 2026, demonstrating sustained activity in the orthopedic surgical implant space. Recent clearances include all-suture anchors, knotless anchor systems, and specialized reconstruction devices for shoulder and foot-and-ankle procedures.

The company's product portfolio encompasses suture anchors for rotator cuff and labral repairs, specialized instruments for shoulder and foot-and-ankle procedures, and the GreenRepair® initiative designed to reduce surgical waste. Tigon Medical continues to expand its offerings in minimally invasive orthopedic surgery techniques.

Explore the full list of device names, product codes, and FDA 510(k) clearance dates in the database.