FDA applicant

Valley Forge Scientific Corp.

Valley Forge, PA27 decisions1980–20051 recall

FDA records 27 decisions for Valley Forge Scientific Corp. (Valley Forge, PA) from 1980 to 2005: 27 510(k) clearances. Most are in product codes GEI (Electrosurgical, Cutting & Coagulation &…) and JOS (Electrode, Electrosurgical). Its devices cite 10 predicates, 5 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, general and plastic surgery panel, where it files most

How often FDA has decided Valley Forge Scientific Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Valley Forge Scientific Corp. since 2007.

Recalls per year

1in 2010

2007high 1 (2010) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Valley Forge Scientific Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Valley Forge Scientific Corp.’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 Contax, Inc. 3 Valley West, Inc. 3 Valley Medical Research, Inc. 1

Valley Forge Scientific Corp.

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?

What has been recalled?

Other applicant names beginning “Valley”