Sonavex, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sonavex, Inc. - FDA 510(k) Cleared Devices
Recent clearances: EchoGuide (Version 1), EchoSure Diagnostic Ultrasound System, EchoMark, EchoMark LP
3
Total
3
Cleared
0
Denied
Sonavex, Inc. has 3 FDA 510(k) cleared medical devices. Based in Baltimore, US.
Latest FDA clearance: Apr 2025. Active since 2018.
Browse the FDA 510(k) cleared devices submitted by Sonavex, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Sonavex, Inc.
3 devices