FDA applicant

Block Drug Company, Inc.

Jersey City, NJ10 decisions1978–19940 recalls

FDA records 10 decisions for Block Drug Company, Inc. (Jersey City, NJ) from 1978 to 1994: 10 510(k) clearances. Most are in product codes EJR (Agent, Polishing, Abrasive, Oral Cavity) and KOT (Carboxymethylcellulose Sodium Or Polyvinyl…). 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 Block Drug Company, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Block Drug Company, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Block Drug Company, 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 “Block”

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

Block Medical, Inc. 12

Block Drug Company, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Block”