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 Mcube Technology with 6 510(k) clearances. The most recent is a 510(k) clearance dated Aug 19, 2020: CUBEScan BioCon-1100.
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 |
|---|---|---|
| Aug 19, 2020 | CUBEScan BioCon-1100K201995 · IYO | 510(k) clearances |
| May 19, 2020 | CUBEScan BioCon-900SK200749 · IYO | 510(k) clearances |
| Mar 27, 2020 | CUBEScan BioCon-1100K200548 · IYO | 510(k) clearances |
| Jun 22, 2017 | CUBEScan™ BioCon-900 (Bladder Volume Measurement System)K171591 · IYO | 510(k) clearances |
| Apr 27, 2011 | CUBESCAN / BIOCON-700K111021 · ITX | 510(k) clearances |
| Jun 18, 2009 | CUBESCAN BIOCON-500 DIAGNOSTIC ULTRASOUND SYSTEMK091518 · IYO | 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
