Wipak OY

FDA Regulatory Profile

Wipak OY appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Jun 7, 2024.

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K232625Steriking® Pouch for Robotic InstrumentsJun 7, 2024
K231996Steriking® LT-Blueline Pouches with Tyvek®Sep 7, 2023
K231999Steriking® LT-Blueline Pouches with Tyvek®Sep 7, 2023
K221379Steriking LT-Blueline Pouches with TyvekJan 4, 2023
K221377SteriKing LT-Blueline Pouches with TyvekDec 22, 2022
K221016Steriking Packaging for Medical DevicesMay 5, 2022
K210810Steiking Packaging for Medical DevicesJan 23, 2022