Lorvic Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lorvic Corp. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Lorvic Corp. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1976 to 1987. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Lorvic Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lorvic Corp.
6 devices
Cleared
Sep 11, 1987
U. V. GERMICIDAL UNIT
General Hospital
137d
Cleared
May 03, 1978
SHIELD
Dental
75d
Cleared
Jan 14, 1977
DISP. ABSORBENT COMPRESSED FIBRE WAFER
Dental
3d
Cleared
Jan 14, 1977
FLUORIDE GEL DISPOSABLE TRAY
Dental
3d
Cleared
Sep 21, 1976
SALIVA EJECTOR
Dental
8d
Cleared
Jul 16, 1976
IMPULSE HEAT SEALER
Dental
18d