Medical Device Manufacturer · US , Mchenry , IL

Lee Pharmaceuticals - FDA 510(k) Cleared Devices

29 submissions · 29 cleared · Since 1976

Recent clearances: RESTOBOND 4, PRECISE(R) BETA QUARTZ GLASS-CERAMIC INSERT, LEE-FISCHER CERAMIC REINFORCED PLASTIC BRACKETS

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29

Total

29

Cleared

0

Denied

FDA 510(k) Regulatory Record - Lee Pharmaceuticals Dental ✕

29 devices

1-12 of 29

Cleared Mar 31, 1993

Cleared Jul 24, 1991

PRECISE(R) BETA QUARTZ GLASS-CERAMIC INSERT

Cleared Jun 28, 1990

LEE-FISCHER CERAMIC REINFORCED PLASTIC BRACKETS

Cleared Oct 31, 1989

RESTOBOND 3/DENTIN-ENAMEL BONDING AGENT

Cleared Jul 01, 1988

Cleared Jan 20, 1988

LEE COMPOSITE INLAY SYSTEM

Cleared Sep 25, 1986

RESTODENT POSTERIOR

Cleared Jan 30, 1986

PROTEC/VISIBLE LIGHT-CURED SEALANT/DENTAL RESTORAT

Cleared Jan 04, 1985

CLEANSE N BOND I

Cleared Jan 04, 1985

CLEANSE N BOND II

Cleared Oct 25, 1984

Cleared Jun 27, 1984

RESTODENT DENTIN BONDING AGENT