Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in DenmarkLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Innovision A/S with 10 510(k) clearances and 1 device recall. The most recent is a device recall dated May 13, 2016: Innocor Cardiopulmonary Exercise and Lung Function Testing System Non-invasive diag….
| May 13, 2016 | Innocor Cardiopulmonary Exercise and Lung Function Testing System Non-invasive diagnostic device that measures or calculates a number oClass II · The purpose of the recall is to replace data transmission cable (USB-cable) connecting the lnnocor device with an extern | Device recalls |
| Jul 24, 2015 | N-Force Fixation SystemK151146 · HWC | 510(k) clearances |
| Mar 6, 2014 | N-FORCE FIXATION SYSTEMK132244 · HWC | 510(k) clearances |
| Nov 1, 2011 | LCI OPTION FOR INNOCORK102047 · BZC | 510(k) clearances |
| Jul 28, 2011 | N-FORCE FIXATION SYSTEMK102528 · HWC | 510(k) clearances |
| Feb 23, 2009 | INNOCOR ERGOSPIROMETRY SYSTEM (INN00010), THE BASIC INNOCOR INCLUDING BREATH-BY-BREATH SYSTEM (INN00400), NIBP(INN00500)K083879 · BZG | 510(k) clearances |
| Sep 7, 2007 | CARDIOPULMONARY EXERCISE TESTING OPTION TO INNOCORK071911 · DQK | 510(k) clearances |
| Mar 2, 2006 | INNOCORK051907 · DQK | 510(k) clearances |
| Jul 27, 2001 | HYDRO2, HS-75K011914 · HQD | 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
