Lee Pharmaceuticals is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lee Pharmaceuticals - FDA 510(k) Cleared Devices
29
Total
29
Cleared
0
Denied
Lee Pharmaceuticals has 29 FDA 510(k) cleared dental devices. Based in Mchenry, US.
Historical record: 29 cleared submissions from 1976 to 1993.
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 - Lee Pharmaceuticals
29 devices
Cleared
Mar 31, 1993
RESTOBOND 4
Dental
212d
Cleared
Jul 24, 1991
PRECISE(R) BETA QUARTZ GLASS-CERAMIC INSERT
Dental
63d
Cleared
Jun 28, 1990
LEE-FISCHER CERAMIC REINFORCED PLASTIC BRACKETS
Dental
127d
Cleared
Oct 31, 1989
RESTOBOND 3/DENTIN-ENAMEL BONDING AGENT
Dental
109d
Cleared
Jul 01, 1988
PROSTHODENT VL
Dental
56d
Cleared
Jan 20, 1988
LEE COMPOSITE INLAY SYSTEM
Dental
163d
Cleared
Sep 25, 1986
RESTODENT POSTERIOR
Dental
41d
Cleared
Jan 30, 1986
PROTEC/VISIBLE LIGHT-CURED SEALANT/DENTAL RESTORAT
Dental
55d
Cleared
Jan 04, 1985
CLEANSE N BOND I
Dental
73d
Cleared
Jan 04, 1985
CLEANSE N BOND II
Dental
73d
Cleared
Oct 25, 1984
RESTODENT VL
Dental
58d
Cleared
Jun 27, 1984
RESTODENT DENTIN BONDING AGENT
Dental
127d