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 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list USGI Medical with 13 510(k) clearances. The most recent is a 510(k) clearance dated Jan 14, 2011: G-PROX EZ ENDOSCOPIC GRASPER.
| Jan 14, 2011 | G-PROX EZ ENDOSCOPIC GRASPERK103688 · OCZ | 510(k) clearances |
| Dec 30, 2010 | G-CINCH SUTURE GRASPERK102931 · OCW | 510(k) clearances |
| Oct 20, 2010 | G-CATH TISSUE ANCHOR DELIVERY CATHETERK102916 · GAT | 510(k) clearances |
| Feb 17, 2010 | G-CATH TISSUE ANCHOR DELIVERY CATHETER, MODELS 205302, 205333K100251 · GAT | 510(k) clearances |
| Oct 7, 2009 | G-PROX ENDOSCOPIC GRASPER, MODEL 205333K093018 · GAT | 510(k) clearances |
| Sep 13, 2007 | USGI TRANSPORT ENDOSCOPIC ACCESS DEVICEK072405 · FED | 510(k) clearances |
| Dec 6, 2006 | G-PROX ENDOSCOPIC GRASPERK061276 · GAT | 510(k) clearances |
| Jul 31, 2006 | G-LIX TISSUE GRASPERK061268 · HET | 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
