510(k) Report

FDA applicant

Aspect Vision Care, Ltd.

Freehold, NJ5 decisions1997–19991 recall

FDA records 5 decisions for Aspect Vision Care, Ltd. (Freehold, NJ) from 1997 to 1999: 5 510(k) clearances. All are in product code LPL (Lenses, Soft Contact, Daily Wear). Its devices cite 7 predicates, 2 of them its own earlier devices. 1 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 Aspect Vision Care, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Aspect Vision Care, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Aspect Vision Care, 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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Other applicant names beginning “Aspect”

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