Reimers and Janssen GmbH is one of 218 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Reimers and Janssen GmbH - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Reimers and Janssen GmbH has 2 FDA 510(k) cleared medical devices. Based in Berlin, DE.
Historical record: 2 cleared submissions from 2009 to 2014. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Reimers and Janssen GmbH Filter by specialty or product code using the sidebar.
Reimers and Janssen GmbH — FDA 510(k) Products and Clearance History
2 devices
Cleared
Jun 13, 2014
PHYSIOLASER OLYMPIC, SINGLE PROBES CW, CLUSTER PROBES CW, LIGHT NEEDLE,...
Physical Medicine
445d
Cleared
Dec 15, 2009
LASERPEN PRACTISE AND EXPERT, HANDYLASER SPRINT, HANDYLASER TRION,...
Physical Medicine
189d