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Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Doctor'S Research Group, Inc. · Predicate Candidate Screening

13 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

188 daysmedian FDA review time
235 days90th percentile
13clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K051487DRG LARYNGEAL AUGMENTATION IMPLANT DEVICEDoctor'S Research Group, Inc.2005-12-221990
K041018DRG SOFTRELEASEDoctor'S Research Group, Inc.2004-10-181810
K012535DRG DISPOSABLE VAGINAL SPECULUMDoctor'S Research Group, Inc.2002-03-012060
K012003DRG REACTION CHAMBER/SAFETY TIPDoctor'S Research Group, Inc.2002-02-122300
K011736DRG QUICKMIXDoctor'S Research Group, Inc.2002-01-302390
K013786DRG ORTHOHEX SS BONE SCREWDoctor'S Research Group, Inc.2001-12-17330
K002047DRG PURETONE STETHOSCOPE WITH DRG ANTIMICROBIAL, STETHOSCOPEDoctor'S Research Group, Inc.2000-11-221390
K991714DRG CONVENTIONAL ELECTRONIC DIGITAL STETHOSCOPE, MODEL ECHOPDoctor'S Research Group, Inc.1999-12-102040
K990212LOCKJAW 15 MINUTE INTERMAXILLARY FIXATION SYSTEM,MODEL LJ100Doctor'S Research Group, Inc.1999-09-142350
K990920DRG TITANIUM BONE PLATEDoctor'S Research Group, Inc.1999-06-10840
K981881DRG SHERLOCK MF BONE SCREW, COCRMO SELF-TAPPING, TI ALLOY SEDoctor'S Research Group, Inc.1998-12-021880
K982169SHERLOCK THREADED SUTURE ANCHOR (TIN COATED)Doctor'S Research Group, Inc.1998-09-14870
K974817DRG MF TITANIUN ALLOY BONE SCREW 1.0MM, 1.2MM, 1.3MM, 1.5MM,Doctor'S Research Group, Inc.1998-03-13800

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda