USpharma, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
USpharma, Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
USpharma, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Miami Lakes, US.
Latest FDA clearance: Jun 2026. Active since 2026. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by USpharma, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - USpharma, Ltd.
1 devices