Medical Device Manufacturer · US , Mchenry , IL

Coe Laboratories, Inc. - FDA 510(k) Cleared Devices

20 submissions · 20 cleared · Since 1976

Total

Cleared

Denied

Coe Laboratories, Inc. has 20 FDA 510(k) cleared dental devices. Based in Mchenry, US.

Historical record: 20 cleared submissions from 1976 to 1990.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

Coe Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Coe Laboratories, Inc.

20 devices

1-12 of 20

Cleared Oct 19, 1990

ACCUFLEX/ACCUMIX VINYL POLY IMPRESSION MATERIALS

FIRST IMPRESSION WITH CHLORHEXIDINE

K894281 · ELW

Dental · 95d

Cleared May 01, 1989

OCCLU-SEAL(TM) VISIBLE LIGHT-CURED FISSURE SEALANT

K891140 · EBC

Dental · 59d

Cleared Feb 13, 1989

TRIPTON(TM) VISIBLE LIGHT-CURED UNIV. BONDING

K885010 · KLE

Dental · 73d

Cleared Oct 31, 1988

COE PAK AUTO MIX, REGULAR OR HARD SET

K881422 · EMA

Dental · 209d

Cleared Jun 28, 1988

OMNISIL, VINYL POLYSILOXANE IMPRESSION MATERIAL

K881091 · ELW

Dental · 112d

Cleared Nov 18, 1986

OPALUX VISIBLE LIGHT CURED ANTERIOR COMPOSITE

K863882 · EBF

Dental · 43d

Cleared Mar 11, 1985

ABSOLUTE VINYL POLYSILOXANE IMPRESS

K842877 · ELW

Dental · 231d

Cleared Dec 11, 1984

COE-LITE POLYMERIZATION UNIT

K844325 · EBZ

Dental · 34d

Cleared Dec 03, 1984

OCCLUSIN LIGHT CURED VISIBLE RADIOPAQUE COMPOSITE

General Hospital · 349d

Coe Laboratories, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Coe Laboratories, Inc.

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