Stoneheart, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stoneheart, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Stoneheart, Inc. has 1 FDA 510(k) cleared medical devices. Based in Cheney, US.
Historical record: 1 cleared submissions from 1993 to 1993. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Stoneheart, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Stoneheart, Inc.
1 devices