FDA applicant

Valley Contax, Inc.

Springfield, OR3 decisions2017–20220 recalls

FDA records 3 decisions for Valley Contax, Inc. (Springfield, OR) from 2017 to 2022: 3 510(k) clearances. All are in product code HQD (Lens, Contact (Other Material) - Daily). Since 2016 its 510(k)s took a median of 50 days from receipt to decision, against 66 for FDA’s reviews in the same codes and years. Its devices cite 6 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 Valley Contax, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2022

2017high 1 (2017) · low 0 (2018)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2017.

FIG. 1 — Valley Contax, Inc. by year, 2017–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Valley Contax, Inc.’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 “Valley”

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

Valley Forge Scientific Corp. 27 Valley West, Inc. 3 Valley Medical Research, Inc. 1

Valley Contax, Inc.

Which product codes does it file in?

How long do its 510(k) reviews take?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Valley”