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 15, 2026, FDA's public records list Dornoch Medical Systems with 6 510(k) clearances. The most recent is a 510(k) clearance dated Apr 24, 2019: IntelliCartTM System.
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.
| Apr 24, 2019 | IntelliCartTM SystemK190789 · JCX | 510(k) clearances |
| Sep 14, 2017 | IntelliCart SystemK172481 · JCX | 510(k) clearances |
| Dec 21, 2016 | IntelliCartTM SystemK162421 · JCX | 510(k) clearances |
| Mar 21, 2014 | DORNOCH DUO SUCTION CART WITH: DL2800 LID, CL500 LID, DORNOCH QUAD SUCTION CART WITH: DL2800 LID, CL500 LIDK133786 · JCX | 510(k) clearances |
| Mar 4, 2013 | DORNOCH DUO SUCTION CART WITH DL2800 LID MODEL UL-DU2800, DORNOCH DUO SUCTION CART WITH CL500 LID MODEL UL-DU500, DORNOCK123188 · JCX | 510(k) clearances |
| Apr 29, 2008 | TRANSPOSAL ULTRA SYSTEMSK081047 · JCX | 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
