Xpan, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Xpan, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Xpan Universal Trocar System
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.
FDA 510(k) Regulatory Record - Xpan, Inc.
1 devices