Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Clarus Medical Systems with 22 510(k) clearances. The most recent is a 510(k) clearance dated Aug 18, 1998: CLARUS ENDOSCOPIC DISCECTOMY SYSTEM SITETRAC MODEL 6000.
| Aug 18, 1998 | CLARUS ENDOSCOPIC DISCECTOMY SYSTEM SITETRAC MODEL 6000K980588 · GAD | 510(k) clearances |
| Feb 18, 1998 | PERCSCOPE MODEL 2600K974579 · HRX | 510(k) clearances |
| May 23, 1997 | CLARUS MODEL 2127-900 SERIES ENDOSCOPE ADATER (2127-900 SERIES)K971584 · OCV | 510(k) clearances |
| May 20, 1997 | CLARUS MODEL 5197 SIGHTLITEK971455 · FTI | 510(k) clearances |
| Dec 24, 1996 | CLARUS NEUROPEN ENDOSCOPIC PLACEMENT KIT MODEL 2125-XXXK960915 · GWG | 510(k) clearances |
| Sep 11, 1996 | CLARUS MURPHYPEN ENDOSCOPE(2127-XXX)K962255 · EOB | 510(k) clearances |
| Feb 6, 1996 | CLARUS SPINEPEN MODEL 2126K955598 · GWG | 510(k) clearances |
| Oct 12, 1995 | INSTRUMENT SCOPEK953685 · GWG | 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
