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.

510(k) submissions have been managed by Medical Device Academy, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - 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