FDA applicant
Doctor'S Research Group, Inc.
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
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.
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.
See the 510(k) Report