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 Siemens HealthineersLabelled 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 Corindus, Inc. with 9 510(k) clearances. The most recent is a 510(k) clearance dated Jul 27, 2022: CorPath GRX System.
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 |
|---|---|---|
| Jul 27, 2022 | CorPath GRX SystemK221464 · DXX | 510(k) clearances |
| Dec 11, 2020 | CorPath GRX SystemK202275 · DXX | 510(k) clearances |
| Mar 29, 2018 | CorPath GRX SystemK180517 · DXX | 510(k) clearances |
| Mar 1, 2018 | CorPath GRX SystemK173806 · DXX | 510(k) clearances |
| Feb 15, 2018 | CorPath GRX SystemK173288 · DXX | 510(k) clearances |
| Oct 27, 2016 | CorPath GRX SystemK160121 · DXX | 510(k) clearances |
| Mar 18, 2016 | CorPath 200 SystemK152999 · DXX | 510(k) clearances |
| Oct 2, 2015 | CorPath 200 SystemK150892 · DXX | 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
