Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of HeraeusLabelled 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 Heraeus Medical Components with 4 510(k) clearances. The most recent is a 510(k) clearance dated Dec 19, 2019: Hereaeus Poseidon Microcatheter.
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.
| Dec 19, 2019 | Hereaeus Poseidon MicrocatheterK191305 · KRA | 510(k) clearances |
| Nov 26, 2019 | Heraeus Peripheral GuidewireK191502 · DQX | 510(k) clearances |
| Nov 9, 2017 | Odyssey Micro CatheterK170664 · DQY | 510(k) clearances |
| Oct 20, 2017 | Heraeus TMW GuidewireK173052 · 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
