Operart, LLC is one of 18469 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Operart, LLC - FDA 510(k) Cleared Devices
Recent clearances: Prodigio Stain Powder
1
Total
1
Cleared
0
Denied
Operart, LLC has 1 FDA 510(k) cleared medical devices. Based in Santa Monica, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Operart, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Insight, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Operart, LLC
1 devices