P&A USA is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
P&A USA - FDA 510(k) Cleared Devices
Recent clearances: HEXIM Implant
1
Total
1
Cleared
0
Denied
P&A USA has 1 FDA 510(k) cleared medical devices. Based in Annadale, US.
Latest FDA clearance: Jul 2025. Active since 2025. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by P&A USA Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Rook Quality Systems as regulatory consultant.
FDA 510(k) Regulatory Record - P&A USA
1 devices