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 Evergreen Technologies with 7 510(k) clearances. The most recent is a 510(k) clearance dated Dec 7, 1994: MEDVISION ENVIROMENT/MEDVISION 2.0.
| Date | Record | Source |
|---|---|---|
| Dec 7, 1994 | MEDVISION ENVIROMENT/MEDVISION 2.0K942861 · LMD | 510(k) clearances |
| Sep 16, 1994 | VISIONLINK DICOM MODULEK942860 · KPS | 510(k) clearances |
| Feb 9, 1994 | VISIONLINK ACR-NEMA CONVERSION UTILITIESK935103 · LMD | 510(k) clearances |
| Nov 1, 1993 | VISIONLINK INTERFILE CONVERSION SOFTWAREK933372 · KPS | 510(k) clearances |
| Sep 29, 1993 | VISIONTOOLK933209 · LLZ | 510(k) clearances |
| Feb 2, 1993 | MEDVISION(TM) IMAGING SOFTWAREK924178 · LMD | 510(k) clearances |
| Aug 7, 1992 | MEDVISIONK921484 · LLZ | 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
