Mk-Dent GmbH is one of 516 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Mk-Dent GmbH - FDA 510(k) Cleared Devices
Recent clearances: MK-DENT LOW SPEED HANDPIECES AND ACCESSORIES INCLUDING SPARE PARTS, TUBINGS, AND LIGHT POWER SYSTEM, MODELS: LS2011, MK-DENT HIGH SPEED DENTAL HANDPIECE, MODELS HS 4021K, 4011K, 4012K, AND HS 6021K, 6011K, 6012K
2
Total
2
Cleared
0
Denied
Mk-Dent GmbH has 2 FDA 510(k) cleared medical devices. Based in Kumhausen, DE.
Historical record: 2 cleared submissions from 2003 to 2005. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Mk-Dent GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mk-Dent GmbH
2 devices