Ulab Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ulab Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: uLab Systems Dental Aligner Kit, ULab Systems uDesign Software, ULab Systems Dental Aligner Kit
4
Total
4
Cleared
0
Denied
Ulab Systems, Inc. has 4 FDA 510(k) cleared medical devices. Based in Menlo Park, US.
Last cleared in 2022. Active since 2018. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Ulab Systems, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Sylvia Erickson Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Ulab Systems, Inc.
4 devices