American Eagle Instruments, Inc. is one of 5240 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Eagle Instruments, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
American Eagle Instruments, Inc. has 2 FDA 510(k) cleared medical devices. Based in Missoula, US.
Historical record: 2 cleared submissions from 2005 to 2013. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by American Eagle Instruments, Inc. Filter by specialty or product code using the sidebar.
American Eagle Instruments, Inc. — FDA 510(k) Products and Clearance History
2 devices
Cleared
Mar 29, 2013
AEI DR. TERAUCHI ULTRASONIC TIPS
Dental
225d
Cleared
Mar 18, 2005
XP TECHNOLOGY ULTRASONIC SCALER
Dental
141d