Slow Wave, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Slow Wave, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Slow Wave DS8 (SWDS802), Slow Wave DS8
2
Total
2
Cleared
0
Denied
Slow Wave, Inc. has 2 FDA 510(k) cleared medical devices. Based in Spicewood, US.
Latest FDA clearance: Jun 2024. Active since 2020. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Slow Wave, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Slow Wave, Inc.
2 devices