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 13, 2026, FDA's public records list Medi-Globe with 26 510(k) clearances. The most recent is a 510(k) clearance dated Apr 16, 2026: Endoflux™ Biliary & Pancreatic Stent Sets.
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 |
|---|---|---|
| Apr 16, 2026 | Endoflux™ Biliary & Pancreatic Stent SetsK251658 · FGE | 510(k) clearances |
| May 19, 2016 | EasyPass GuidewireK153264 · OCY | 510(k) clearances |
| Sep 30, 2014 | PolyCatch Retrieval DeviceK142258 · FDI | 510(k) clearances |
| May 15, 2014 | SONOTIP PRO AND PRO FLEX EBUS-TBNA NEEDLE SYSTEMK133763 · FCG | 510(k) clearances |
| May 8, 2009 | MEDI-GLOBE SONOTIP II EBUS-TBNA NEEDLE SYSTEMK091257 · FCG | 510(k) clearances |
| Mar 20, 2009 | SONOTIP II 25-GAUGE ULTRASOUND NEEDLE SYSTEM, MODELS GUS-01-18-025 AND GUS-01-27-025K083802 · FCG | 510(k) clearances |
| Jan 31, 2007 | SONOTIP II ULTRASOUND NEEDLE SYSTEMK070129 · FCG | 510(k) clearances |
| Jul 3, 2006 | INJECTRA INJECTION NEEDLEK061222 · FBK | 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
