FDA applicant

Novo Nordisk Pharmaceuticals, Inc.

Princeton, NJ2 decisions1993–19950 recalls

FDA records 2 decisions for Novo Nordisk Pharmaceuticals, Inc. (Princeton, NJ) from 1993 to 1995: 2 510(k) clearances. All are in product code FMF (Syringe, Piston). 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 Novo Nordisk Pharmaceuticals, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Novo Nordisk Pharmaceuticals, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Novo”

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

Novo Nordisk, Inc. 14 Novo Nordisk Diagnostics, Ltd. 2 Novo Diagnostic Systems 2 Novo Norodisk Pharmaceuticals, Inc. 1 Novo Nordisk A/S 1

Novo Nordisk Pharmaceuticals, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Novo”