FDA applicant

Preventive Technologies, Inc.

Charlotte, NC3 decisions1995–20140 recalls

FDA records 3 decisions for Preventive Technologies, Inc. (Charlotte, NC) from 1995 to 2014: 3 510(k) clearances. Most are in product codes EHK (Cup, Prophylaxis) and LBH (Varnish, Cavity). Its devices cite 2 predicates, 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 Preventive Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2014

2007high 1 (2010) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Preventive Technologies, 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

Other applicant names beginning “Preventive”

FDA records each applicant name separately; these may or may not be the same firm.

Preventive Diagnostics Corp. 18 Preventive Care, Inc. 3 Preventive Medicine Institute 1

Preventive Technologies, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Preventive”