Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Case Medical with 16 510(k) clearances. The most recent is a 510(k) clearance dated Jun 3, 2026: SteriTite Container System with MediTray Products.
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.
| Jun 3, 2026 | SteriTite Container System with MediTray ProductsK252854 · KCT | 510(k) clearances |
| Jul 31, 2024 | SteriTite rigid reusable sterilization container with MediTray ProductsK240898 · KCT | 510(k) clearances |
| Oct 7, 2022 | SteriTite Container System with MediTray PartsK221492 · KCT | 510(k) clearances |
| Apr 29, 2022 | SteriTite Container System with MediTray ProductsK212711 · KCT | 510(k) clearances |
| Jun 13, 2018 | Case Medical SteriTite Reusable Rigid Sterilization Container System with MediTray accessoriesK173259 · KCT | 510(k) clearances |
| Feb 10, 2017 | SteriTite Containers System & MediTray ProductsK161415 · FRG | 510(k) clearances |
| Jan 24, 2012 | STERITEC CONTAINERS SYSTEM & MEDITRAY PRODUCTSK112904 · FRG | 510(k) clearances |
| Jul 1, 2011 | STERITITE CONTAINER SYSTEM & MEDITRAY PRODUCTSK110682 · KCT | 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
