510(k) Report

FDA applicant

Doctor'S Research Group, Inc.

Wolcott, CT13 decisions1998–20050 recalls

FDA records 13 decisions for Doctor'S Research Group, Inc. (Wolcott, CT) from 1998 to 2005: 13 510(k) clearances. Most are in product codes DZL (Screw, Fixation, Intraosseous) and DQD (Stethoscope, Electronic). Its devices cite 6 predicates, 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 Doctor'S Research Group, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Doctor'S Research Group, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Doctor'S Research Group, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Doctor'S Research Group, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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