Nexus6, Ltd. is one of 32 FDA 510(k) medical device manufacturers from New Zealand in the dataset, ranked by real submission volume.
Nexus6, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: SMARTTOUCH, SMARTTRACK SYSTEM
2
Total
2
Cleared
0
Denied
Nexus6, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Auckland, NZ.
Historical record: 2 cleared submissions from 2009 to 2014. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Nexus6, Ltd. 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 - Nexus6, Ltd.
2 devices