FDA applicant

Euclid Vision Corporation

Sterling1 decision2004–20040 recalls

FDA records 1 decision for Euclid Vision Corporation (Sterling) in 2004: 1 original PMA approval. All are in product code NUU (Lens, Contact, Orthokeratology, Overnight). 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 Euclid Vision Corporation’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Euclid Vision Corporation since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Other applicant names beginning “Euclid”

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

Euclid Systems Corp. 1

Euclid Vision Corporation

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Euclid”