Brazen Goods Inc. Dba Lorals is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Brazen Goods Inc. Dba Lorals - FDA 510(k) Cleared Devices
Recent clearances: Lorals
1
Total
1
Cleared
0
Denied
Brazen Goods Inc. Dba Lorals has 1 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Last cleared in 2022. Active since 2022. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Brazen Goods Inc. Dba Lorals Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Acknowledge Regulatory Strategies, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Brazen Goods Inc. Dba Lorals
1 devices