Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Doctors Research Group with 14 510(k) clearances. The most recent is a 510(k) clearance dated Nov 16, 2009: KRYPTONITE BONE CEMENT.
| Nov 16, 2009 | KRYPTONITE BONE CEMENTK091382 · GXP | 510(k) clearances |
| Dec 22, 2005 | DRG LARYNGEAL AUGMENTATION IMPLANT DEVICEK051487 · KHJ | 510(k) clearances |
| Oct 18, 2004 | DRG SOFTRELEASEK041018 · HHT | 510(k) clearances |
| Mar 1, 2002 | DRG DISPOSABLE VAGINAL SPECULUMK012535 · HIB | 510(k) clearances |
| Feb 12, 2002 | DRG REACTION CHAMBER/SAFETY TIPK012003 · HEI | 510(k) clearances |
| Jan 30, 2002 | DRG QUICKMIXK011736 · GXP | 510(k) clearances |
| Dec 17, 2001 | DRG ORTHOHEX SS BONE SCREWK013786 · HWC | 510(k) clearances |
| Nov 22, 2000 | DRG PURETONE STETHOSCOPE WITH DRG ANTIMICROBIAL, STETHOSCOPE DIAPHRAGM, MODEL PT2B27(CARDIOLOGY), PT3B27(CLASSIC), PT5B2K002047 · DQD | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
