Medical Device Manufacturer · US , Falls Church , VA

Artech Corp. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1984

8

Total

8

Cleared

0

Denied

FDA 510(k) Regulatory Record - Artech Corp. Dental ✕

8 devices

1-8 of 8

Cleared Mar 05, 1992

ARTECH ARDENT IV - TYPE CLYLINDER IMPLANT

Cleared Apr 10, 1990

ARTECH TYPE SS-HA SUBMERGED SCREW IMPLANT

Cleared Dec 21, 1989

ARTECH TYPE SS SUBMERGED SCREW IMPLANT

Cleared Sep 28, 1989

HAND TOOLS FOR ARTECH TYPE SS SUBMERGED SCREW IMPL

Cleared Sep 27, 1989

COUNTERBORE FOR SS SUBMERGED SCREW PLANT

Cleared Sep 27, 1989

IRRIGATED DRILL FOR SS SUBMERGED SCREW PLANT

Cleared Oct 15, 1984

HOLLOW BASKET DENTAL IMPLANTS

Cleared Sep 27, 1984

TPS SCREW DENTAL IMPLANTS

Data Source

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

Last updated: Apr 27, 2026