USpharma, Ltd. is one of 16362 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
USpharma, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Curajel™ Oral Gel
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.
510(k) submissions have been managed by Eliquent Life Sciences, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - USpharma, Ltd.
1 devices