Homtex, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Homtex, Inc. has 2 FDA 510(k) cleared medical devices. Based in Cullman, US.
Last cleared in 2021. Active since 2021. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Homtex, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Homtex, Inc.
2 devices