Wipak Oy
Nastola, FI
Wipak OY appears in FDA device records in Nastola, FI. FDA records list 7 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 7
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 7 510(k) clearances for Wipak Oy between 2022 and 2024. The busiest year on record is 2022, with 3. The most recent is 2024, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2022 | 3 |
| 2023 | 3 |
| 2024 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K232625 | Steriking® Pouch for Robotic Instruments | FRG | Substantially Equivalent | |
| K231999 | Steriking® LT-Blueline Pouches with Tyvek® | FRG | Substantially Equivalent | |
| K231996 | Steriking® LT-Blueline Pouches with Tyvek® | FRG | Substantially Equivalent | |
| K221379 | Steriking LT-Blueline Pouches with Tyvek | FRG | Substantially Equivalent | |
| K221377 | SteriKing LT-Blueline Pouches with Tyvek | FRG | Substantially Equivalent | |
| K221016 | Steriking Packaging for Medical Devices | FRG | Substantially Equivalent | |
| K210810 | Steiking Packaging for Medical Devices | FRG | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain