Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Control Medical Technology with 5 510(k) clearances. The most recent is a 510(k) clearance dated Mar 24, 2025: VentiV 7Fr -12Fr MP Mechanical Thrombectomy System (VS7-MP60S, VS7-MP90S, VS8-MP60S, VS8….
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.
| Mar 24, 2025 | VentiV 7Fr -12Fr MP Mechanical Thrombectomy System (VS7-MP60S, VS7-MP90S, VS8-MP60S, VS8-MP90S, VS8-MP100B, VS10-MP100B, VS11-MP60S, VS11-MP90S, VS12-MP100B, 7F-MP60S, 7F-MP90S, 8F-MP60S, 8F-MP100B, 10F-MP100B, 11F-MP60S, 11F-MP90S, 11P-MP60S, 11P-MP90S, 12F-MP100B, V30-ASP)K250013 · QEZ | 510(k) clearances |
| May 29, 2020 | Aspire Mechanical Aspirator GK200629 · FMF | 510(k) clearances |
| May 4, 2020 | Aspire MAX 7 - 11F Mechanical Thrombectomy System and Aspire Mechanical AspiratorK200871 · QEZ | 510(k) clearances |
| Nov 26, 2013 | ASPIRE RX-LP6 ASPIRATION CATHETERK131998 · QEZ | 510(k) clearances |
| Feb 22, 2012 | ASPIRE MAX ASPIRATION CATHETERK113757 · QEZ | 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
