Xerothera, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Xerothera, Inc. has 1 FDA 510(k) cleared medical devices. Based in West Chester, US.
Latest FDA clearance: Jun 2024. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Xerothera, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MCRA as regulatory consultant.
1 devices