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 14, 2026, FDA's public records list Vizionfocus with 5 510(k) clearances. The most recent is a 510(k) clearance dated Sep 10, 2025: VizionFocus (somofilcon A) Silicone Hydrogel Soft (hydrophilic) Contact Lens.
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.
| Sep 10, 2025 | VizionFocus (somofilcon A) Silicone Hydrogel Soft (hydrophilic) Contact LensK251573 · LPL | 510(k) clearances |
| Apr 10, 2025 | Aurora (ocufilcon D) Soft (Hydrophilic) Daily Wear Contact Lens (Tinted, Color)K243953 · LPL | 510(k) clearances |
| Dec 17, 2024 | VizionFocus (mififilcon A) Silicone Hydrogel Soft (hydrophilic) Daily Disposable Contact Lens; VizionFocus Color (mififilcon A) Silicone Hydrogel Soft (hydrophilic) Daily Disposable Contact LensK242413 · LPL | 510(k) clearances |
| Dec 9, 2019 | Legacy (Ocufilcon D) Performance- Tinted Soft (Hydrophilic) Daily Wear Contact LensesK192225 · LPL | 510(k) clearances |
| Oct 12, 2018 | ILICON (ocufilcon D) Soft (Hydrophilic) Daily Wear Contact Lenses (Tinted, Color)K182247 · LPL | 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
