Luminex Corp. is one of 508 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Luminex Corp. - FDA 510(k) Cleared Devices
Recent clearances: FLEXMAP 3D, LUMINEX FLEXMAP 3D INSTRUMENT SYSTEM, LUMINEX XPONENT 4.0 SPI SOFTWARE, FLEXMAP 3D IVD CALIBRATION KIT, FLEXMAP 3D IVD P, LUMINEX LX 100/200 INSTRUMENT
3
Total
3
Cleared
0
Denied
Luminex Corp. has 3 FDA 510(k) cleared medical devices. Based in Toronto, CA.
Historical record: 3 cleared submissions from 2008 to 2014.
Browse the FDA 510(k) cleared devices submitted by Luminex Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Luminex Corp.
3 devices