Medical Device Manufacturer · US , Falls Church , VA

Artech Corp. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1984

Total

Cleared

Denied

Artech Corp. has 8 FDA 510(k) cleared medical devices. Based in Falls Church, US.

Historical record: 8 cleared submissions from 1984 to 1992. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Artech Corp. Filter by specialty or product code using the sidebar.

Artech Corp. 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 - Artech Corp.

8 devices

1-8 of 8

Cleared Mar 05, 1992

ARTECH ARDENT IV - TYPE CLYLINDER IMPLANT

K911735 · DZE

Dental · 323d

Cleared Apr 10, 1990

ARTECH TYPE SS-HA SUBMERGED SCREW IMPLANT

K895267 · DZE

Dental · 230d

Cleared Dec 21, 1989

ARTECH TYPE SS SUBMERGED SCREW IMPLANT

K891346 · DZE

Dental · 286d

Cleared Sep 28, 1989

HAND TOOLS FOR ARTECH TYPE SS SUBMERGED SCREW IMPL

K894160 · DZE

Dental · 106d

Cleared Sep 27, 1989

COUNTERBORE FOR SS SUBMERGED SCREW PLANT

K894150 · DZJ

Dental · 105d

Cleared Sep 27, 1989

IRRIGATED DRILL FOR SS SUBMERGED SCREW PLANT

K894151 · DZJ

Dental · 105d

Cleared Oct 15, 1984

HOLLOW BASKET DENTAL IMPLANTS

K843217 · DZE

Dental · 61d

Cleared Sep 27, 1984

TPS SCREW DENTAL IMPLANTS

K843218 · DZE

Dental · 43d

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Apr 27, 2026

Artech Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Artech Corp.

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