Vertos Medical, Inc. - FDA 510(k) Cleared Devices
Vertos Medical, Inc. develops orthopedic devices with a manufacturing facility in Aliso Viejo, California. The company specializes in minimally invasive spine surgery solutions.
Vertos Medical has received 1 FDA 510(k) clearance from 1 total submission. The company's regulatory activity is focused entirely on orthopedic devices. The latest clearance was in 2024, confirming active development and market engagement.
The company's cleared device portfolio includes the Vertos mild Device Kit (MDK-0002), a minimally invasive lumbar decompression system designed to relieve pain and improve mobility in patients with spinal stenosis. This technology reflects Vertos Medical's commitment to advanced surgical solutions in the spine market.
Explore the complete regulatory record, including device names, product codes, and clearance dates in the FDA 510(k) database.