Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Vision Quest Industries with 8 510(k) clearances. The most recent is a 510(k) clearance dated Nov 16, 2020: Avid CT2.
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.
| Nov 16, 2020 | Avid CT2K202490 · IPF | 510(k) clearances |
| Jun 12, 2019 | Avid IF2K183692 · LIH | 510(k) clearances |
| Mar 23, 2015 | BioniCare Hand SystemK142236 · NYN | 510(k) clearances |
| Nov 13, 2009 | T.E.A.R. TECH3K090532 · IPF | 510(k) clearances |
| Apr 24, 2008 | TARGET STERILE ELECTRODEK072799 · GXY | 510(k) clearances |
| Jul 1, 2004 | FAST START TENS, MODEL FS 3001K041092 · GZJ | 510(k) clearances |
| May 20, 2003 | T.E.A.R. TECH3 MODEL #44TT03K030507 · IPF | 510(k) clearances |
| Sep 14, 1998 | SURGI STIMK982388 · IPF | 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
