Medical Device Manufacturer · FI , Nastola

Wipak OY - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2022

Total

Cleared

Denied

Wipak OY has 7 FDA 510(k) cleared medical devices. Based in Nastola, FI.

Latest FDA clearance: Jun 2024. Active since 2022. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Wipak OY Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Compliance Systems International, LLC and Compliance Systems International.

Wipak OY is one of 32 FDA 510(k) medical device manufacturers from Finland in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Wipak OY

7 devices

1-7 of 7

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: May 09, 2026