Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in South KoreaLabelled 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 Vieworks and its 1 subsidiaries with 60 510(k) clearances. The most recent is a 510(k) clearance dated Jul 31, 2026: 0909FCE, 0909FCE-HS.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Vieworks and its 1 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jul 31, 2026 | 0909FCE, 0909FCE-HSK253800 · MQB | 510(k) clearances |
| Jun 18, 2026 | VIVIX-S 4386W (FXRD-4386WA)K260820 · MQB | 510(k) clearances |
| May 28, 2026 | Bellalun 2D (VDMS-1000S)K254092 · MUE | 510(k) clearances |
| Nov 4, 2025 | VXvueK251410 · LLZ | 510(k) clearances |
| Mar 12, 2025 | 2430TCA with Xmaru WK243849 · MUE | 510(k) clearances |
| Jan 16, 2025 | VIVIX-MK241113 · MUE | 510(k) clearances |
| Nov 15, 2024 | VIVIX-S 1751SK241125 · MQB | 510(k) clearances |
| Sep 9, 2024 | Digital Flat Panel X-ray Detector (1717WCE, 1717WCE-HR, 1717WCE-HS, 1717WCE-GF)K242394 · MQB | 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
