FDA applicant

Vision Science Co., Ltd.

Beaverton, OR2 decisions2014–20160 recalls

FDA records 2 decisions for Vision Science Co., Ltd. (Beaverton, OR) from 2014 to 2016: 2 510(k) clearances. All are in product code LPL (Lenses, Soft Contact, Daily Wear). Its devices cite 5 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 Vision Science Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2014high 1 (2014) · low 0 (2015)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2014.

FIG. 1 — Vision Science Co., Ltd. by year, 2014–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Vision Science Co., Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Vision Science Co., Ltd.

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?