Graftworx, Inc. Dba Alio - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Graftworx, Inc. Dba Alio has 1 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Last cleared in 2022. Active since 2022. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Graftworx, Inc. Dba Alio Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Acknowledge Regulatory Strategies, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Graftworx, Inc. Dba Alio
1 devices