Mti Precision Products is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mti Precision Products - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Mti Precision Products has 5 FDA 510(k) cleared medical devices. Based in Lakewood, US.
Historical record: 5 cleared submissions from 1989 to 2007. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Mti Precision Products Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mti Precision Products
5 devices
Cleared
Feb 02, 2007
MASTER CLASSIC 5K LOW SPEED HANDPIECE, 20K LOW SPEED HANDPIECE, TM5 LOW SPEED...
Dental
30d
Cleared
Mar 28, 1996
LYNX DPA DISPOSABLE PROPHY ANGLE
Dental
50d
Cleared
Dec 29, 1994
LYNX LOW-SPEED HANDPIECE
Dental
342d
Cleared
May 15, 1990
LYNX-SM, SCLAER DENTAL HANDPIECE
Dental
47d
Cleared
Dec 18, 1989
LYNX-HIGH SPEED HANDPIECE
Dental
83d