Tanita Corporation of America is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tanita Corporation of America - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Tanita Corporation of America has 2 FDA 510(k) cleared medical devices. Based in Arlington Heights, US.
Historical record: 2 cleared submissions from 2006 to 2009. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Tanita Corporation of America Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tanita Corporation of America
2 devices