FDA applicant

Foremost Mfg., Inc.

Englewood, NJ1 decision1991–19910 recalls

FDA records 1 decision for Foremost Mfg., Inc. (Englewood, NJ) in 1991: 1 510(k) clearance. All are in product code EBF (Material, Tooth Shade, Resin). 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, dental panel, where it files most

How often FDA has decided Foremost Mfg., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Foremost Mfg., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Foremost Mfg., 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 “Foremost”

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

Foremost Dental Mfg., Inc. 15 Foremost Dental, LLC 1

Foremost Mfg., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Foremost”