Jenoptik Laser, Optik, Systeme GmbH is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Jenoptik Laser, Optik, Systeme GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Jenoptik Laser, Optik, Systeme GmbH has 1 FDA 510(k) cleared medical devices. Based in Coto De Caza, US.
Historical record: 1 cleared submissions from 1998 to 1998. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Jenoptik Laser, Optik, Systeme GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Jenoptik Laser, Optik, Systeme GmbH
1 devices