Sempermed USA, Inc. is one of 25903 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sempermed USA, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LATEX POWDER-FREE EXAMINATION GLOVES BLUE, POLYMER COATED, CONTAINS 50 MICROGRAMS OR LESS OF TOTAL WATER EXTRACTABLE PRO, LATEX POWDERED PATIENT EXAMINATION GLOVE, 200 MICROGRAMS OR LESS
2
Total
2
Cleared
0
Denied
Sempermed USA, Inc. has 2 FDA 510(k) cleared medical devices. Based in Palm Harbor, US.
Historical record: 2 cleared submissions from 2001 to 2001. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Sempermed USA, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sempermed USA, Inc.
2 devices