Company · FI
Wipak OY
FDA 510(k) clearances and medical device recalls filed under this name, 2022 to 2024. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| FRG | Wrap, Sterilization | 7 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jun 7, 2024 | K232625 | Steriking® Pouch for Robotic Instruments Wipak OY, FI | FRG |
| Sep 7, 2023 | K231999 | Steriking® LT-Blueline Pouches with Tyvek® Wipak OY, FI | FRG |
| Sep 7, 2023 | K231996 | Steriking® LT-Blueline Pouches with Tyvek® Wipak OY, FI | FRG |
| Jan 4, 2023 | K221379 | Steriking LT-Blueline Pouches with Tyvek Wipak OY, FI | FRG |
| Dec 22, 2022 | K221377 | SteriKing LT-Blueline Pouches with Tyvek Wipak OY, FI | FRG |
| May 5, 2022 | K221016 | Steriking Packaging for Medical Devices Wipak OY, FI | FRG |
| Jan 23, 2022 | K210810 | Steiking Packaging for Medical Devices Wipak OY, FI | FRG |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||