FDA applicant

The Lahr Consulting Group, Inc.

Mahwah, NJ1 decision1992–19920 recalls

FDA records 1 decision for The Lahr Consulting Group, Inc. (Mahwah, NJ) in 1992: 1 510(k) clearance. All are in product code DZP (Instrument, Diamond, 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 The Lahr Consulting Group, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Lahr Consulting Group, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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The Lahr Consulting Group, Inc.

Which product codes does it file in?

What has FDA decided for it lately?