Tomy, Inc. is one of 16108 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tomy, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ORTHODONTIC PLASTIC BRACKETS AND ACCESSORIES, ORTHODONTIC CERAMIC BRACKETS 1.1, CERAMIN BRACKETS Z
4
Total
4
Cleared
0
Denied
Tomy, Inc. has 4 FDA 510(k) cleared medical devices. Based in Bradenton, US.
Historical record: 4 cleared submissions from 2012 to 2018. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Tomy, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Primus Consulting and Regulatory & Quality Solutions, Inc..
FDA 510(k) Regulatory Record - Tomy, Inc.
4 devices