510(k) Report

FDA applicant

Professional Dental Technologies Therapeutics, Inc.

Batesville, AR1 decision2004–20040 recalls

FDA records 1 decision for Professional Dental Technologies Therapeutics, Inc. (Batesville, AR) in 2004: 1 510(k) clearance. All are in product code EJR (Agent, Polishing, Abrasive, Oral Cavity). Its devices cite 1 predicate, 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 Professional Dental Technologies Therapeutics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Professional Dental Technologies Therapeutics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Professional Dental Technologies…’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 “Professional”

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