510(k) Report

FDA applicant

Fairfax Dental, Inc.

Miami, FL1 decision1991–19910 recalls

FDA records 1 decision for Fairfax Dental, Inc. (Miami, FL) in 1991: 1 510(k) clearance. All are in product code DZM (Needle, Dental). 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 Fairfax Dental, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Fairfax Dental, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Fairfax Dental, 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

Which product codes does it file in?

  • DZMNeedle, Dental1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K910446Stabident Local Anesthesia SystemFairfax Dental, Inc. · 19911cites it

What has FDA decided for it lately?

  • K910446Stabident Local Anesthesia SystemFairfax Dental, Inc. · 1991

The one decision as Fairfax Dental, Inc. →