Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in CanadaLabelled 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 13, 2026, FDA's public records list Halifax Biomedical with 5 510(k) clearances. The most recent is a 510(k) clearance dated Oct 31, 2018: Halifax Imaging Kit.
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.
| Date | Record | Source |
|---|---|---|
| Oct 31, 2018 | Halifax Imaging KitK182880 · KPR | 510(k) clearances |
| Mar 6, 2014 | MODEL-BASED RSA SOFTWAREK133966 · LLZ | 510(k) clearances |
| Jun 1, 2012 | SR SUITE 1.0K121345 · KPR | 510(k) clearances |
| Jun 28, 2011 | HALIFAX BIOMEDICAL TANATLUM BEAD SETK103417 · NEU | 510(k) clearances |
| Aug 21, 2009 | TANTALUM BEAD SET, MODEL P003175K090581 · NEU | 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
