Rowpar Pharmaceuticals, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rowpar Pharmaceuticals, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CloSYS® Dry Mouth Sensitive Mouth Rinse
1
Total
1
Cleared
0
Denied
Rowpar Pharmaceuticals, Inc. has 1 FDA 510(k) cleared medical devices. Based in Bridgewater, US.
Latest FDA clearance: May 2025. Active since 2025. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Rowpar Pharmaceuticals, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Innovative Science Solutions (D.B.A Lumanity) as regulatory consultant.
FDA 510(k) Regulatory Record - Rowpar Pharmaceuticals, Inc.
1 devices