Doctor'S Research Group, Inc.
FDA 510(k) medical device clearances.
Top product codes for Doctor'S Research Group, Inc.
Recent clearances by Doctor'S Research Group, Inc.
- K051487 — DRG LARYNGEAL AUGMENTATION IMPLANT DEVICE
- K041018 — DRG SOFTRELEASE
- K012535 — DRG DISPOSABLE VAGINAL SPECULUM
- K012003 — DRG REACTION CHAMBER/SAFETY TIP
- K011736 — DRG QUICKMIX
- K013786 — DRG ORTHOHEX SS BONE SCREW
- K002047 — DRG PURETONE STETHOSCOPE WITH DRG ANTIMICROBIAL, STETHOSCOPE DIAPHRAGM, MODEL PT2B27(CARDIOLOGY), PT3B27(CLASSIC), PT5B2
- K991714 — DRG CONVENTIONAL ELECTRONIC DIGITAL STETHOSCOPE, MODEL ECHOP 200-00
- K990212 — LOCKJAW 15 MINUTE INTERMAXILLARY FIXATION SYSTEM,MODEL LJ100-00
- K990920 — DRG TITANIUM BONE PLATE
- K981881 — DRG SHERLOCK MF BONE SCREW, COCRMO SELF-TAPPING, TI ALLOY SELF-TAPPING/SELF DRILLING, COCRMO SELF-TAPPING/ SELF DRILLING
- K982169 — SHERLOCK THREADED SUTURE ANCHOR (TIN COATED)
- K974817 — DRG MF TITANIUN ALLOY BONE SCREW 1.0MM, 1.2MM, 1.3MM, 1.5MM, 1.7MM, 2.0MM, 2.4MM
Data sourced from openFDA. This site is unofficial and independent of the FDA.