FirmLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in FinlandLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Wipak Oy with 7 510(k) clearances. The most recent is a 510(k) clearance dated Jun 7, 2024: Steriking® Pouch for Robotic Instruments.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Jun 7, 2024 | Steriking® Pouch for Robotic InstrumentsK232625 · FRG | 510(k) clearances |
| Sep 7, 2023 | Steriking® LT-Blueline Pouches with Tyvek®K231999 · FRG | 510(k) clearances |
| Sep 7, 2023 | Steriking® LT-Blueline Pouches with Tyvek®K231996 · FRG | 510(k) clearances |
| Jan 4, 2023 | Steriking LT-Blueline Pouches with TyvekK221379 · FRG | 510(k) clearances |
| Dec 22, 2022 | SteriKing LT-Blueline Pouches with TyvekK221377 · FRG | 510(k) clearances |
| May 5, 2022 | Steriking Packaging for Medical DevicesK221016 · FRG | 510(k) clearances |
| Jan 23, 2022 | Steiking Packaging for Medical DevicesK210810 · FRG | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
