Jintronix, Inc. is one of 642 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Jintronix, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Jintronix, JINTRONIX REHABILITATION SYSTEM (JRS)
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.
510(k) submissions have been managed by Axsource Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Jintronix, Inc.
2 devices