FDA applicant

Nanova Biomaterials, Inc.

Columbia, MO8 decisions2014–20180 recalls

FDA records 8 decisions for Nanova Biomaterials, Inc. (Columbia, MO) from 2014 to 2018: 8 510(k) clearances. Most are in product codes MAI (Fastener, Fixation, Biodegradable, Soft Tissue) and EBF (Material, Tooth Shade, Resin). Since 2016 its 510(k)s took a median of 160 days from receipt to decision, against 119 for FDA’s reviews in the same codes and years. Its devices cite 12 predicates, 0 of them its own earlier devices. 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 Nanova Biomaterials, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2018

2014high 2 (2015) · low 0 (2019)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2014.

FIG. 1 — Nanova Biomaterials, Inc. by year, 2014–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Nanova Biomaterials, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Nanova Biomaterials, Inc.

Which product codes does it file in?

How long do its 510(k) reviews take?

Whose devices does it build on?

What has FDA decided for it lately?