Bioarchitects USA, LLC is one of 20515 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bioarchitects USA, LLC - FDA 510(k) Cleared Devices
Recent clearances: BioArchitects Patient Specific Cranial/Craniofacial Plate
1
Total
1
Cleared
0
Denied
Bioarchitects USA, LLC has 1 FDA 510(k) cleared medical devices. Based in New York, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Bioarchitects USA, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ferguson Medical International Device Consultants, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Bioarchitects USA, LLC
1 devices