FDA applicant

Northern Implants, LLC

Fairfax, VA4 decisions2004–20060 recalls

FDA records 4 decisions for Northern Implants, LLC (Fairfax, VA) from 2004 to 2006: 4 510(k) clearances. All are in product code DZE (Implant, Endosseous, Root-Form). Its devices cite 28 predicates, 4 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 Northern Implants, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Northern Implants, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Northern Implants, LLC’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

Northern Implants, LLC

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?