FDA applicant

Rohm and Haas Co.

Mchenry, IL4 decisions1982–19910 recalls

FDA records 4 decisions for Rohm and Haas Co. (Mchenry, IL) from 1982 to 1991: 4 510(k) clearances. Most are in product codes EBG (Crown And Bridge, Temporary, Resin) and EBI (Resin, Denture, Relining, Repairing, Rebasing). 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 Rohm and Haas Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rohm and Haas Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Rohm and Haas Co.

Which product codes does it file in?

What has FDA decided for it lately?