Xpan, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Xpan, Inc. has 1 FDA 510(k) cleared medical devices. Based in Vaughan, CA.
Last cleared in 2023. Active since 2023. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Xpan, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Lakeshore Medical Device Consulting, LLC as regulatory consultant.
1 devices