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 its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list MR Instruments, Inc. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Nov 28, 2017: DuoFLEX Coil Suite.
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.
| Date | Record | Source |
|---|---|---|
| Nov 28, 2017 | DuoFLEX Coil SuiteK173290 · MOS | 510(k) clearances |
| Jul 25, 2013 | DUOFLEX COIL SUITE (1.5T)K130706 · MOS | 510(k) clearances |
| Mar 29, 2011 | MC 1504G-16R, 1.5T, 16-CHANNEL, MC 3004G-16R, 3.0T, 16-CHANNEL HEAD COILK110591 · MOS | 510(k) clearances |
| Apr 2, 2008 | TEM 3002G- HN DUAL TUNE HEAD COILK080820 · MOS | 510(k) clearances |
| Oct 30, 2007 | MC 3003G-32R HEAD COILK072931 · MOS | 510(k) clearances |
| Aug 19, 2005 | TEM 3000 HEAD COILK052200 · MOS | 510(k) clearances |
| Apr 23, 2004 | TEM 3000 HEAD COILK040937 · MOS | 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
