FDA applicant

I-See Vision Technology, Inc.

Flagstaff, AZ4 decisions2009–20150 recalls

FDA records 4 decisions for I-See Vision Technology, Inc. (Flagstaff, AZ) from 2009 to 2015: 4 510(k) clearances. All are in product code LPL (Lenses, Soft Contact, Daily Wear). Its devices cite 7 predicates, 1 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 I-See Vision Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2009high 3 (2009) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

FIG. 1 — I-See Vision Technology, Inc. by year, 2009–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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I-See Vision Technology, Inc.

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?