Wipak OY - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
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.
FDA 510(k) cleared devices by Wipak OY
7 devices
Cleared
Jun 07, 2024
Steriking® Pouch for Robotic Instruments
General Hospital
283d
Cleared
Sep 07, 2023
Steriking® LT-Blueline Pouches with Tyvek®
General Hospital
64d
Cleared
Sep 07, 2023
Steriking® LT-Blueline Pouches with Tyvek®
General Hospital
64d
Cleared
Jan 04, 2023
Steriking LT-Blueline Pouches with Tyvek
General Hospital
237d
Cleared
Dec 22, 2022
SteriKing LT-Blueline Pouches with Tyvek
General Hospital
224d
Cleared
May 05, 2022
Steriking Packaging for Medical Devices
General Hospital
30d
Cleared
Jan 23, 2022
Steiking Packaging for Medical Devices
General Hospital
312d