Jintronix, Inc. is one of 209 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Jintronix, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Jintronix, Inc. has 2 FDA 510(k) cleared medical devices. Based in Milton, Ontario, CA.
Historical record: 2 cleared submissions from 2014 to 2015. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Jintronix, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Jintronix, Inc.
2 devices