Puregraft, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Puregraft, LLC - FDA 510(k) Cleared Devices
Recent clearances: Dermapose Access, Dermapose Refresh
2
Total
2
Cleared
0
Denied
Puregraft, LLC has 2 FDA 510(k) cleared medical devices. Based in Solana Beach, US.
Historical record: 2 cleared submissions from 2020 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Puregraft, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Puregraft, LLC
2 devices