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 Aragon Surgical, Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jul 11, 2011: ARAGON SURGICAL RF SYSTEM - 5MM LAPAROSCOPIC INSTRUMENT.
| Jul 11, 2011 | ARAGON SURGICAL RF SYSTEM - 5MM LAPAROSCOPIC INSTRUMENTK110824 · GEI | 510(k) clearances |
| Jan 21, 2010 | ARAGON SURGICAL RF SYSTEM TELEO INSTRUMENTK093075 · GEI | 510(k) clearances |
| Jun 18, 2009 | ARAGON SURGICAL RF SYSTEM L2 INSTRUMENTK090306 · GEI | 510(k) clearances |
| Oct 31, 2008 | ARAGON ONESHOT SYSTEMK081312 · GEI | 510(k) clearances |
| Jan 11, 2008 | MODIFICATION TO: ARAGON SURGICAL LAPCAPK073452 · HIF | 510(k) clearances |
| May 30, 2007 | ARAGON SURGICAL LAPCAPK070651 · HIF | 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
