Medical device makerLabelled 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 nContact Surgical, Inc. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Oct 28, 2014: EPI-SENSE GUIDED COAGULATION DEVICE WITH VISITRAX.
| Oct 28, 2014 | EPI-SENSE GUIDED COAGULATION DEVICE WITH VISITRAXK142084 · OCL | 510(k) clearances |
| Nov 13, 2012 | EPI-SENSE GUIDED COAGULATION DEVICE WITH VISITRAXK120857 · OCL | 510(k) clearances |
| Feb 17, 2009 | NUMERIS GUIDED COAGULATION SYSTEM WITH VISITRAX, MODELS CSK-121, -122, -123 AND -125K090202 · OCL | 510(k) clearances |
| Dec 30, 2008 | NUMERIS COAGULATION SYSTEM WITH VISITRAX, MODEL(S) CSK-021;CSK-022; CSK-023; CSK-025K082203 · OCL | 510(k) clearances |
| Jul 26, 2007 | NCONTACT VISITRAX GUIDED COAGULATION SYSTEM KIT, MODELS CSK-212 AND CSK-515K071819 · OCL | 510(k) clearances |
| Dec 1, 2006 | NCONTACT COAGULATION SYSTEM KITK062539 · GEI | 510(k) clearances |
| Dec 1, 2006 | NCONTACT COAGULATION SYSTEM KIT, MODEL CSKK063012 · OCL | 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
