FDA applicant

Worldwide Dental, Inc.

Clearwater, FL4 decisions1977–19960 recalls

FDA records 4 decisions for Worldwide Dental, Inc. (Clearwater, FL) from 1977 to 1996: 4 510(k) clearances. Most are in product codes IWO (Apron, Protective) and EIE (Dam, Rubber). 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 Worldwide Dental, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Worldwide Dental, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Worldwide Dental, 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 “Worldwide”

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

Worldwide Medical Technologies, LLC 15 Worldwide Medical Corp. 9 Worldwide Surgical Gauze 4

Worldwide Dental, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Worldwide”