Medical Device Manufacturer · US , Liverpool , NY

Pdo Max, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2019
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.

FDA 510(k) cleared devices by Pdo Max, Inc.

2 devices
1-2 of 2
Cleared Dec 17, 2021
PDO Max Suture with Dual Needle
K210871 · NEW
General & Plastic Surgery · 268d
Cleared Jun 04, 2019
PDS Barbed Suture, PDO MAXX Threads
K190245 · NEW
General & Plastic Surgery · 118d
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All2 General & Plastic Surgery 2