Medical Device Manufacturer · US , Central Islip , NY

Gac Intl., Inc. - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 1977

Total

Cleared

Denied

Gac Intl., Inc. has 13 FDA 510(k) cleared dental devices. Based in Central Islip, US.

Historical record: 13 cleared submissions from 1977 to 1999.

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

Gac Intl., 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 - Gac Intl., Inc.

13 devices

1-13 of 13

ORTHODONITC METAL REINFORCED PLASTIC BRACKET

MICROARCH GOLD BRACKET

K932825 · EJF

Dental · 334d

Cleared Sep 20, 1993

ORTHODONTIC ELASTOMER

K932319 · ECI

Dental · 132d

Cleared Sep 13, 1993

ION-IMPLANTED NEO SENTALLOY

ORTHODONTIC STAINLESS STEEL BRACKET

K923029 · EJF

Dental · 97d

Cleared Aug 24, 1992

GAC THUMB-SUCKING CONTROL APPLIANCE

K920850 · DZC

Dental · 181d

Cleared Mar 20, 1992

ORTHODONTIC FACE BOW W/ INNER WIRE

K920784 · DZB

Dental · 29d

Cleared Aug 20, 1985

CERAMIC ORTHODONIT APPLIANCE

K852179 · EJF

Dental · 92d

Cleared May 09, 1985

SENTINOL -ORTHODONTIC ARCH WIRE

K851055 · DZC

Dental · 56d

Cleared Sep 30, 1977

NEW BASE FOR ORTHODONTIC APPLIANCES

K771774 · EJF

Dental · 11d

Gac Intl., Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Gac Intl., Inc.

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