FDA applicant

Park Dental Research Corp.

Ardmore, OK8 decisions1986–20260 recalls

FDA records 8 decisions for Park Dental Research Corp. (Ardmore, OK) from 1986 to 2026: 8 510(k) clearances. Most are in product codes DZE (Implant, Endosseous, Root-Form) and NXC (Aligner, Sequential). Since 2016 its 510(k)s took a median of 113 days from receipt to decision, against 107 for FDA’s reviews in the same codes and years. Its devices cite 13 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Park Dental Research Corporation”.

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 Park Dental Research Corp.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2025

2007high 1 (2010) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Park Dental Research Corp.’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 “Park”

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

Park Medical Systems, Inc. 2

Park Dental Research Corp.

Which product codes does it file in?

How long do its 510(k) reviews take?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Park”