Westport Medical, Inc. is one of 24558 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Westport Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: POWERTOME PERIOTOME
1
Total
1
Cleared
0
Denied
Westport Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Salem, US.
Historical record: 1 cleared submissions from 2006 to 2006. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Westport Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Westport Medical, Inc.
1 devices