Medical device makerLabelled 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 13, 2026, FDA's public records list HDC S.r.l. with 33 510(k) clearances. The most recent is a 510(k) clearance dated Jul 30, 2009: HDC STERILE SELF LIGATING SPIDER SCREW, MODEL SLI,SL2.
| Date | Record | Source |
|---|---|---|
| Jul 30, 2009 | HDC STERILE SELF LIGATING SPIDER SCREW, MODEL SLI,SL2K091390 · OAT | 510(k) clearances |
| Nov 5, 2007 | V-CATH POLY PICCK071875 · LJS | 510(k) clearances |
| Oct 18, 2007 | HDC STERILE SPIDER SCREWK071851 · DZE | 510(k) clearances |
| Dec 23, 2005 | HDC SPIDER SCREWK052471 · DZE | 510(k) clearances |
| Mar 2, 2004 | NEURO-TRACE III KIT, NEURO-TRACE III REGIONAL BLOCK CABLE, NEURO-TRACE III NERVE MAPPING PROBE, NEURO-TRACE III NERVE BGK023342 · KOI | 510(k) clearances |
| Jan 14, 2004 | MODIFICATION TO V-CATH POLY PICCK033853 · FOZ | 510(k) clearances |
| Sep 10, 2003 | SELDINGER SAFETY NEEDLE INTRODUCERK032404 · DYB | 510(k) clearances |
| Sep 9, 2003 | PANDIN CONTINUOUS NERVE STIMULATING CATHETER, MODELS 561-18-05, 561-18-09, 561-18-15, 562-18-05, 562-18-09 & 562-18-15K022752 · CAZ | 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
