510(k) Report

FDA applicant

Foremost Dental Mfg., Inc.

Englewood, NJ15 decisions1985–19980 recalls

FDA records 15 decisions for Foremost Dental Mfg., Inc. (Englewood, NJ) from 1985 to 1998: 15 510(k) clearances. Most are in product codes EBF (Material, Tooth Shade, Resin) and EMA (Cement, Dental). Its devices cite 1 predicate, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Foremost Dental Mfg., Co.”.

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 Dental Mfg., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Foremost Dental Mfg., Inc.’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 “Foremost”

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