510(k) Report

FDA applicant

Ab Ardent

Tonawanda, NY13 decisions1998–20130 recalls

FDA records 13 decisions for Ab Ardent (Tonawanda, NY) from 1998 to 2013: 13 510(k) clearances. Most are in product codes EBF (Material, Tooth Shade, Resin) and EJJ (Alloy, Amalgam). Its devices cite 1 predicate, 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 Ab Ardent’s devices, and how often a recall has named them.

FDA decisions per year

1in 2013

2013: 1
2007high 1 (2013) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report