Keos is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Keos - FDA 510(k) Cleared Devices
Recent clearances: Keos Anterior Cervical Interbody Fusion Device System, Keos Lumbar IBFD
4
Total
4
Cleared
0
Denied
Keos, is a medical device company with a manufacturing facility in Lancaster, US. The company specializes in Orthopedic devices for spinal fusion and interbody fusion applications.
Keos received 4 FDA 510(k) clearances from 4 total submissions between 2016 and 2022. The company's regulatory portfolio is entirely focused on Orthopedic devices, including anterior cervical and lumbar interbody fusion systems. Keos is currently inactive with no clearances recorded in the past five years and should be treated as a historical regulatory record.
For detailed information on cleared device names, product codes, and clearance dates, review the company's complete 510(k) submission history.
Regulatory submissions have been managed by Mrc-X, LLC and MRC Global, LLC.
FDA 510(k) Regulatory Record - Keos
4 devices