Medical device makerLabelled 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 Medcom GmbH with 11 510(k) clearances. The most recent is a 510(k) clearance dated Sep 21, 2018: VeriSuite.
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 |
|---|---|---|
| Sep 21, 2018 | VeriSuiteK181789 · LHN | 510(k) clearances |
| Mar 27, 2018 | PreludeK180308 · MUJ | 510(k) clearances |
| Jul 26, 2017 | BiopSee, Mobile USK170841 · LLZ | 510(k) clearances |
| May 1, 2017 | NaviSuite SSI EditionK163119 · LLZ | 510(k) clearances |
| Apr 3, 2014 | VERISUITE 1.8, VERISUITE-PARTICLE 1.8, VERISUITE, VERISUITE-PARTICLEK133914 · LHN | 510(k) clearances |
| Nov 23, 2010 | PVS MODEL 1.0K102237 · IYE | 510(k) clearances |
| May 7, 2010 | MEDCOM RT-VIEWER SYSTEMK100056 · MUJ | 510(k) clearances |
| Sep 18, 2009 | VERISUITE AND VERISUITE-PARTICLE, VERSION 1.8K092653 · LHN | 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
