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 Mecta Corporation with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jun 4, 2021: ECT Cotton Bite Block- size Large, ECT Cotton Bite Block -size Medium.
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 4, 2021 | ECT Cotton Bite Block- size Large, ECT Cotton Bite Block -size MediumK201309 · JXL | 510(k) clearances |
| Apr 26, 2020 | MECTA SigmaK192834 · QGH | 510(k) clearances |
| Mar 6, 1997 | SPECTRUM 5000 Q, 5000Q,M,4000 Q, 4000 M.K965070 · QGH | 510(k) clearances |
| Sep 18, 1996 | SPECTRUM 5000 Q, 5000 M, 4000 Q, 4000 MK960754 · QGH | 510(k) clearances |
| Aug 9, 1985 | MECTA ECT DEVICE MODELS SR & JRK852069 · QGH | 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
