Pdo Max, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pdo Max, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PDO Max Suture with Dual Needle, PDS Barbed Suture, PDO MAXX Threads
2
Total
2
Cleared
0
Denied
Pdo Max, Inc. has 2 FDA 510(k) cleared medical devices. Based in Liverpool, US.
Last cleared in 2021. Active since 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Pdo Max, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Medical Device Academy, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Pdo Max, Inc.
2 devices