Customfab, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Customfab, Inc. has 1 FDA 510(k) cleared medical devices. Based in Garden Grove, US.
Last cleared in 2021. Active since 2021. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Customfab, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by leanRAQA, LLCx as regulatory consultant.
1 devices