Dmetec.Co., Ltd. is one of 18450 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dmetec.Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: COMPACT S, COMPACT S (LED), ULTRASONIC SURGERY, ULTRASONIC SURGERY MACHINE
5
Total
5
Cleared
0
Denied
Dmetec.Co., Ltd. has 5 FDA 510(k) cleared medical devices. Based in Great Neck, US.
Historical record: 5 cleared submissions from 2005 to 2017. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Dmetec.Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Onbix Corporation as regulatory consultant.
FDA 510(k) Regulatory Record - Dmetec.Co., Ltd.
5 devices