FDA applicant

Whitehill Oral Technologies, Inc.

Hazlet, NJ2 decisions1995–19960 recalls

FDA records 2 decisions for Whitehill Oral Technologies, Inc. (Hazlet, NJ) from 1995 to 1996: 2 510(k) clearances. All are in product code JES (Floss, 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 Whitehill Oral Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Whitehill Oral Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Whitehill Oral 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 “Whitehill”

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

Whitehill Manufacturing, Inc. 1

Whitehill Oral Technologies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Whitehill”