Maxx Digm, Inc. is one of 18423 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Maxx Digm, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Zmaxx T Series
1
Total
1
Cleared
0
Denied
Maxx Digm, Inc. has 1 FDA 510(k) cleared medical devices. Based in Santa Clara, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Maxx Digm, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by LK Consulting Group USA, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Maxx Digm, Inc.
1 devices