Vestibular First is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vestibular First - FDA 510(k) Cleared Devices
Recent clearances: Insight Infrared Video Goggles
1
Total
1
Cleared
0
Denied
Vestibular First has 1 FDA 510(k) cleared medical devices. Based in Broomall, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Vestibular First Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Vestibular First
1 devices