Ajk Engineering, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ajk Engineering, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Lotus Prophy Angle
1
Total
1
Cleared
0
Denied
Ajk Engineering, Inc. has 1 FDA 510(k) cleared medical devices. Based in Sommerville, US.
Last cleared in 2022. Active since 2022. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Ajk Engineering, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MRC Global, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Ajk Engineering, Inc.
1 devices