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 14, 2026, FDA's public records list Medeon Biodesign, Inc. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Apr 30, 2020: ClickClean.
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 30, 2020 | ClickCleanK200902 · GCJ | 510(k) clearances |
| Mar 26, 2020 | AbClose - Port Site Closure DeviceK193652 · OCW | 510(k) clearances |
| Nov 7, 2019 | Laparoscope Lens Shield Device (LENS)K192891 · GCJ | 510(k) clearances |
| Feb 16, 2017 | Laparoscope Lens Shield Device (LENS)K170103 · GCJ | 510(k) clearances |
| Sep 9, 2016 | AbClose - Port Site Closure DeviceK160117 · OCW | 510(k) clearances |
| Apr 21, 2016 | Laparoscope Lens Shield DeviceK160172 · GCJ | 510(k) clearances |
| Aug 20, 2015 | Laparoscope Lens Shield DeviceK151117 · GCJ | 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
