FDA applicant

Allegheny Plastics, Inc.

Coraopolis, PA1 decision1987–19870 recalls

FDA records 1 decision for Allegheny Plastics, Inc. (Coraopolis, PA) in 1987: 1 510(k) clearance. All are in product code HMM (Distometer). 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, ophthalmic panel, where it files most

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

FDA decisions per year

No FDA decision for Allegheny Plastics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Allegheny Plastics, Inc.

Which product codes does it file in?

What has FDA decided for it lately?