FDA applicant

Nunc, Inc.

Riverside, CA3 decisions1987–19870 recalls

FDA records 3 decisions for Nunc, Inc. (Riverside, CA) in 1987: 3 510(k) clearances. Most are in product codes KJA (Flask, Tissue Culture) and KIZ (Dish, Tissue Culture). 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, hematology panel, where it files most

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

FDA decisions per year

No FDA decision for Nunc, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Nunc, 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 “Nunc”

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

Nunc A/S 2

Nunc, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Nunc”