FDA applicant

Soflex Isralens Contact Lens, Ltd.

20184 Misgav, IL1 decision2002–20020 recalls

FDA records 1 decision for Soflex Isralens Contact Lens, Ltd. (20184 Misgav, IL) in 2002: 1 510(k) clearance. All are in product code LPL (Lenses, Soft Contact, Daily Wear). 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 Soflex Isralens Contact Lens, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Soflex Isralens Contact Lens, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Soflex Isralens Contact Lens, Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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See the 510(k) Report

Other applicant names beginning “Soflex”

FDA records each applicant name separately; these may or may not be the same firm.

Soflex Contact Lens Industries, Ltd. 6 Soflex Limited 3

Soflex Isralens Contact Lens, Ltd.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Soflex”