Lares Manufacturing Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lares Manufacturing Co., Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Lares Manufacturing Co., Inc. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1978 to 1983. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Lares Manufacturing Co., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lares Manufacturing Co., Inc.
6 devices
Cleared
Nov 14, 1983
PERMALUX VISIBLE CURE COMPOSITE RESTOR
Dental
203d
Cleared
Dec 16, 1980
LARES HANDPIECE OIL
Dental
166d
Cleared
Jul 21, 1980
FIBER OPTIC ILLUMINATOR
Dental
10d
Cleared
Jul 21, 1980
FIBER OPTIC HOSE
Dental
10d
Cleared
Jul 14, 1980
LARES AIR PRESSURE GAUGE
Dental
11d
Cleared
Jan 20, 1978
DENTAL HANDPIECE
Dental
11d