Preventive Technologies, Inc. is one of 5098 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Preventive Technologies, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Preventive Technologies, Inc. has 3 FDA 510(k) cleared medical devices. Based in Charlotte, US.
Historical record: 3 cleared submissions from 1995 to 2014. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Preventive Technologies, Inc. Filter by specialty or product code using the sidebar.
Preventive Technologies, Inc. — FDA 510(k) Products and Clearance History
3 devices
Cleared
Dec 12, 2014
VELLA 5% SODIUM FLUORIDE VARNISH WITH NUFLUOR AND XYLITOL
Dental
304d
Cleared
Jun 17, 2010
PREVENTECH PROPHYLAXIS PASTE WITH FLUORIDE
Dental
112d
Cleared
May 02, 1995
DISPOSABLE PROPHYLAXIS ANGLE
Dental
57d