Progressive Technology, Inc. is one of 5098 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Progressive Technology, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Progressive Technology, Inc. has 3 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 3 cleared submissions from 1981 to 2015. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Progressive Technology, Inc. Filter by specialty or product code using the sidebar.
Progressive Technology, Inc. — FDA 510(k) Products and Clearance History
3 devices
Cleared
May 15, 2015
Chi Lites Orthodontic Sapphire Bracket
Dental
234d
Cleared
Aug 13, 1990
AURA CERAMIC DENTAL APPLIANCE
Dental
75d
Cleared
Oct 13, 1981
AMPLITONE-3
Cardiovascular
21d