FDA applicant

Glederer & Co., Inc.

Paterson, NJ2 decisions1996–19960 recalls

FDA records 2 decisions for Glederer & Co., Inc. (Paterson, NJ) in 1996: 2 510(k) clearances. All are in product code LDQ (Unnamed device). 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, general hospital panel, where it files most

How often FDA has decided Glederer & Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Glederer & Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Glederer & Co., Inc.

Which product codes does it file in?

What has FDA decided for it lately?