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 Medical Device Technologies with 46 510(k) clearances. The most recent is a 510(k) clearance dated Aug 27, 2010: BIOPINCE ULTRA FULL CORE BIOPSY INSTRUMENT.
| Aug 27, 2010 | BIOPINCE ULTRA FULL CORE BIOPSY INSTRUMENTK101832 · KNW | 510(k) clearances |
| Jan 26, 2006 | INTERV BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHORK053518 · NEU | 510(k) clearances |
| Aug 30, 2005 | INTER V BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHORK051421 · NEU | 510(k) clearances |
| May 26, 2005 | CANALIZER HYDROPHILIC GUIDE WIREK050873 · DQX | 510(k) clearances |
| Feb 11, 2005 | INTERV BRAND SNARELOK BONE MARROW BIOPSY NEEDLEK043523 · KNW | 510(k) clearances |
| Sep 30, 2004 | V-CORE FULL CORE BREAST BIOPSY INSTRUMENTK042464 · KNW | 510(k) clearances |
| May 3, 2004 | FIBREX CATHETER PATENCY DEVICEK040427 · FOZ | 510(k) clearances |
| Aug 13, 2003 | PBN GUIDEWIRESK031442 · DQX | 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
