510(k) Report

FDA applicant

Aalba Dent, Inc.

Fairfield, CA27 decisions1985–20040 recalls

FDA records 27 decisions for Aalba Dent, Inc. (Fairfield, CA) from 1985 to 2004: 27 510(k) clearances. Most are in product codes EJH (Alloy, Metal, Base) and EJT (Alloy, Gold-Based Noble Metal). 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 Aalba Dent, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Aalba Dent, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Aalba Dent, Inc.’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