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 MK Meditech with 6 510(k) clearances. The most recent is a 510(k) clearance dated Dec 19, 2021: ATOZ Mini-Screw.
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.
| Dec 19, 2021 | ATOZ Mini-ScrewK210559 · OAT | 510(k) clearances |
| Apr 5, 2005 | INSOSAFE BAK'SNAP RETRACTABLE INSULIN SAFETY SYRINGEK050131 · MEG | 510(k) clearances |
| Jan 21, 2004 | 10 ML BAK'SNAP DUOPROSS RETRACTABLE SAFETY SYRINGEK034031 · MEG | 510(k) clearances |
| Jun 6, 2003 | BAK'SNAP DUOPRO SAFETY SYRING (DUOPROSS) SAFETY'TRAY ALLERGY SAFETY SYRINGE TRAYK031594 · MEG | 510(k) clearances |
| Sep 19, 2002 | DUOPRO SAFETY SYRINGE (DUOPROSS)K022806 · MEG | 510(k) clearances |
| May 2, 2002 | DUOPRO SAFETY SYRINGE (DUOPROSS)K020623 · MEG | 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
