FDA applicant

Dent Corp. Research & Development

White Plains, NY3 decisions1999–20070 recalls

FDA records 3 decisions for Dent Corp. Research & Development (White Plains, NY) from 1999 to 2007: 3 510(k) clearances. Most are in product codes EBZ (Activator, Ultraviolet, For Polymerization) and LQY (Locator, Root Apex). 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 Dent Corp. Research & Development’s devices, and how often a recall has named them.

FDA decisions per year

1in 2007

2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Dent Corp. Research & Development’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 “Dent”

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

Dent Zar, Inc. 12 Dent-Dr. 1 Dent'N CO 1 Dent-X Co. 1

Dent Corp. Research & Development

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Dent”