Pulsenmore, Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Pulsenmore, Ltd. - FDA 510(k) Cleared Devices
1
Total
0
Cleared
1
Denied
Pulsenmore, Ltd. has 0 FDA 510(k) cleared medical devices. Based in Omer, IL.
Active since 2025. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Pulsenmore, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pulsenmore, Ltd.
1 devices