Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in IsraelLabelled 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 13, 2026, FDA's public records list Etview Ltd. with 9 510(k) clearances. The most recent is a 510(k) clearance dated Nov 29, 2018: VivaSight-SL (TVT) system.
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 |
|---|---|---|
| Nov 29, 2018 | VivaSight-SL (TVT) systemK181880 · BTR | 510(k) clearances |
| Nov 14, 2018 | VivaSight-DL SystemK181886 · CBI | 510(k) clearances |
| Feb 25, 2016 | ETView VivaSight-SL (TVT) systemK152438 · BTR | 510(k) clearances |
| Apr 15, 2013 | VIVASIGHT-DL SYSTEMK123853 · CBI | 510(k) clearances |
| Jun 21, 2012 | ETVIEW TRACHEOSCOPIC VENTILATION TUBE (TVT(TM))K121028 · BTR | 510(k) clearances |
| Jun 8, 2012 | VIVA EBK120334 · CBI | 510(k) clearances |
| May 18, 2012 | DOUBLE LUMEN VIDEO TRACHEOSDOPE (DLVT) SYSTEMK113576 · CBI | 510(k) clearances |
| Oct 8, 2008 | TRACHEOSCOPIC VENTILATION TUBE (TVT)K082420 · BTR | 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
