Enlightenvue, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Enlightenvue, Inc. - FDA 510(k) Cleared Devices
Recent clearances: EnlightenVue Microendoscopy System
1
Total
1
Cleared
0
Denied
Enlightenvue, Inc. has 1 FDA 510(k) cleared medical devices. Based in Denver, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Enlightenvue, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Alira Health as regulatory consultant.
FDA 510(k) Regulatory Record - Enlightenvue, Inc.
1 devices