Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in IsraelLabelled 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 UltraGuide with 6 510(k) clearances. The most recent is a 510(k) clearance dated Oct 22, 2002: USG 2000SA.
| Oct 22, 2002 | USG 2000SAK023227 · HHJ | 510(k) clearances |
| Aug 13, 2002 | ULTRAGUIDE CTG 2000SAK022354 · JAK | 510(k) clearances |
| Oct 18, 2001 | MR-GUIDE 2000K013150 · LNH | 510(k) clearances |
| May 24, 2001 | ULTRAGUIDE MR-GUIDE 3000K011418 · LNH | 510(k) clearances |
| Aug 8, 2000 | ULTRAGUIDE CT-GUIDE 1010K002258 · JAK | 510(k) clearances |
| Feb 9, 1998 | ULTRAGUIDE 1000K974432 · IYO | 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
