Litton Dental Products is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Litton Dental Products - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Litton Dental Products has 12 FDA 510(k) cleared dental devices. Based in Mchenry, US.
Historical record: 12 cleared submissions from 1976 to 1979.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Litton Dental Products
12 devices
Cleared
Oct 26, 1979
MASTERSCALE II
Dental
59d
Cleared
Sep 17, 1979
ULTRASONIC DENTAL PROPHYLAXIS UNIT
Dental
110d
Cleared
Aug 14, 1978
ULTRAMATE 990
Dental
42d
Cleared
Jun 30, 1978
ULTRASONIC DENTAL PROPHYLAXIS UNIT,SSM
Dental
8d
Cleared
Jan 20, 1978
ILLUMINATED DENTAL HANDPIECE
Dental
42d
Cleared
Aug 22, 1977
EXR
Dental
10d
Cleared
Aug 19, 1977
ULTRASON 990
Dental
7d
Cleared
Jul 15, 1977
HU:500, HYGIENASSIST
Dental
4d
Cleared
Jul 15, 1977
CB600, TURBINE CONTROL BOL
Dental
4d
Cleared
Dec 16, 1976
SONUS III
Dental
3d
Cleared
Dec 16, 1976
LT:200, LOVING TOUCH
Dental
3d
Cleared
Aug 11, 1976
TURBINE, AIR DRIVEN HANDPIECE (2000)
Dental
14d