Medical device makerLabelled 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 Micron Corporation with 5 510(k) clearances. The most recent is a 510(k) clearance dated Mar 8, 2018: AW-100.
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.
| Mar 8, 2018 | AW-100K171150 · ELC | 510(k) clearances |
| Dec 22, 2016 | Y-MICK161639 · ELC | 510(k) clearances |
| Mar 28, 2014 | QUICK JET MK133170 · EFB | 510(k) clearances |
| Nov 20, 2003 | SSS, MODEL 1072001 (STANDARD 4-HOLE MODEL) & 1072002 (STANDARD 2-HOLE MODEL)K032995 · ELC | 510(k) clearances |
| Oct 18, 1999 | VIP 60 (2H), MODEL 115-000-1, VIP 60 (4H), MODEL 115-000-2K991239 · ELC | 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
