Doctor'S Research Group, Inc. is one of 13015 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Doctor'S Research Group, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DRG LARYNGEAL AUGMENTATION IMPLANT DEVICE, DRG CONVENTIONAL ELECTRONIC DIGITAL STETHOSCOPE, MODEL ECHOP 200-00, LOCKJAW 15 MINUTE INTERMAXILLARY FIXATION SYSTEM,MODEL LJ100-00
13
Total
13
Cleared
0
Denied
Doctor'S Research Group, Inc. has 13 FDA 510(k) cleared medical devices. Based in Wolcott, US.
Historical record: 13 cleared submissions from 1998 to 2005.
Browse the FDA 510(k) cleared devices submitted by Doctor'S Research Group, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Doctor'S Research Group, Inc.
13 devices
Cleared
Dec 22, 2005
DRG LARYNGEAL AUGMENTATION IMPLANT DEVICE
Ear, Nose, Throat
199d
Cleared
Oct 18, 2004
DRG SOFTRELEASE
Obstetrics & Gynecology
181d
Cleared
Mar 01, 2002
DRG DISPOSABLE VAGINAL SPECULUM
Obstetrics & Gynecology
206d
Cleared
Feb 12, 2002
DRG REACTION CHAMBER/SAFETY TIP
Obstetrics & Gynecology
230d
Cleared
Jan 30, 2002
DRG QUICKMIX
General & Plastic Surgery
239d
Cleared
Dec 17, 2001
DRG ORTHOHEX SS BONE SCREW
Orthopedic
33d
Cleared
Nov 22, 2000
DRG PURETONE STETHOSCOPE WITH DRG ANTIMICROBIAL, STETHOSCOPE DIAPHRAGM, MODEL...
Cardiovascular
139d
Cleared
Dec 10, 1999
DRG CONVENTIONAL ELECTRONIC DIGITAL STETHOSCOPE, MODEL ECHOP 200-00
Cardiovascular
204d
Cleared
Sep 14, 1999
LOCKJAW 15 MINUTE INTERMAXILLARY FIXATION SYSTEM,MODEL LJ100-00
Dental
235d
Cleared
Jun 10, 1999
DRG TITANIUM BONE PLATE
Dental
84d
Cleared
Dec 02, 1998
DRG SHERLOCK MF BONE SCREW, COCRMO SELF-TAPPING, TI ALLOY SELF-TAPPING/SELF...
Dental
188d
Cleared
Sep 14, 1998
SHERLOCK THREADED SUTURE ANCHOR (TIN COATED)
Orthopedic
87d