FDA applicant

Hydrogel Vision Corporation

Sarasota, FL2 decisions2005–20050 recalls

FDA records 2 decisions for Hydrogel Vision Corporation (Sarasota, FL) in 2005: 2 510(k) clearances. All are in product code LPL (Lenses, Soft Contact, Daily Wear). Its devices cite 2 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, ophthalmic panel, where it files most

How often FDA has decided Hydrogel Vision Corporation’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Hydrogel Vision Corporation since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Hydrogel Vision Corporation by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Hydrogel Vision Corporation

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?