Ototronix, LLC is one of 15071 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ototronix, LLC - FDA 510(k) Cleared Devices
Recent clearances: PROCEM, NYSTAGRAM VIDEO NYSTAGMOGRAPHY SYSTEM
2
Total
2
Cleared
0
Denied
Ototronix, LLC has 2 FDA 510(k) cleared medical devices. Based in St. Paul, US.
Historical record: 2 cleared submissions from 2013 to 2014. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Ototronix, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ototronix, LLC
2 devices