Preat Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Preat Corporation - FDA 510(k) Cleared Devices
Recent clearances: Preat Abutments, Preat Abutments, Preat Abutments
3
Total
3
Cleared
0
Denied
Preat Corporation has 3 FDA 510(k) cleared medical devices. Based in Grover Beach, US.
Latest FDA clearance: May 2025. Active since 2019. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Preat Corporation Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by PaxMed International, LLC and Aclivi, LLC.
FDA 510(k) Regulatory Record - Preat Corporation
3 devices