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 Roxwood Medical with 8 510(k) clearances. The most recent is a 510(k) clearance dated Mar 7, 2017: CenterCross Ultra LV Catheter.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Mar 7, 2017 | CenterCross Ultra LV CatheterK170403 · DQY | 510(k) clearances |
| Jun 17, 2016 | CenterCross Ultra CatheterK160681 · DQY | 510(k) clearances |
| Mar 4, 2016 | MultiCross CatheterK152957 · DQY | 510(k) clearances |
| Jan 26, 2016 | CenterCross Ultra CatheterK152456 · DQY | 510(k) clearances |
| Jun 7, 2015 | MicroCross CatheterK151082 · DQY | 510(k) clearances |
| Apr 14, 2015 | MicroCross CatheterK143744 · DQY | 510(k) clearances |
| Nov 19, 2014 | CENTERCROSS CATHETERK140910 · DQY | 510(k) clearances |
| Nov 27, 2012 | MULTICROSS SUPPORT CATHETERK121763 · DQY | 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
