Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in IrelandLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of STERISLabelled 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 15, 2026, FDA's public records list Steris Corporations with 7 510(k) clearances. The most recent is a 510(k) clearance dated Jan 8, 2021: BioGuard Air/Water and Suction Valves.
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.
| Jan 8, 2021 | BioGuard Air/Water and Suction ValvesK203630 · ODC | 510(k) clearances |
| Mar 22, 2019 | SYSTEM 1E Liquid Chemical Sterilant Processing System, SYSTEM 1 Endo Liquid Chemical Sterilant Processing SystemK190104 · MED | 510(k) clearances |
| Jan 4, 2019 | Celerity HP Chemical Indicator (CI)K183295 · JOJ | 510(k) clearances |
| Jan 3, 2019 | VERIFY V24 Self-Contained Biological Indicator, VERIFY V24 Biological Indicator Challenge PackK183300 · FRC | 510(k) clearances |
| Nov 20, 2018 | VERIFY All-In-One STEAM Reusable Test Pack, VERIFY All-In-One STEAM Reusable Test Pack with Step Counter, VERIFY All-In-One STEAM Reusable Test Pack with Tracker TagK182931 · FRC | 510(k) clearances |
| Apr 4, 2018 | SYSTEM 1E Liquid Chemical Sterilant Processing SystemK180342 · MED | 510(k) clearances |
| Feb 9, 2018 | VERIFY V24 Self-Contained Biological Indicator, VERIFY V24 Biological Indicator Challenge PackK172748 · FRC | 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
