Medical Device Manufacturer · US , Windom , MN

Paden Foudry , Ltd. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1991
1
Total
1
Cleared
0
Denied

Paden Foudry , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Windom, US.

Historical record: 1 cleared submissions from 1991 to 1991. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Paden Foudry , Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Paden Foudry , Ltd.

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