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 Viora, Ltd. with 11 510(k) clearances. The most recent is a 510(k) clearance dated Dec 9, 2020: V30 system, V20 system, V10 system, V-VR Hand piece.
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 |
|---|---|---|
| Dec 9, 2020 | V30 system, V20 system, V10 system, V-VR Hand pieceK202247 · PBX | 510(k) clearances |
| Jul 15, 2020 | V30 System, V20 System, V10 System, V-FR HandpieceK201064 · PBX | 510(k) clearances |
| May 21, 2020 | V30 system, V20 system, V10 system, V-FC HandpieceK200468 · PBX | 510(k) clearances |
| Nov 18, 2016 | V30 system, V-Form Handpiece BC Medium applicatorK162363 · GEX | 510(k) clearances |
| Feb 19, 2016 | V20 systemK152611 · GEX | 510(k) clearances |
| May 1, 2015 | V10 systemK150035 · PBX | 510(k) clearances |
| Nov 14, 2014 | V20 SYSTEMK142093 · GEX | 510(k) clearances |
| Oct 21, 2014 | VIORA V-TOUCHK141904 · GEI | 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
