ClearanceBrief
Company ยท US

Artech Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1984 to 1992. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DZEImplant, Endosseous, Root-Form6
DZJDriver, Wire, And Bone Drill, Manual2

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 5, 1992K911735ARTECH ARDENT IV - TYPE CLYLINDER IMPLANT
Artech Corp.
DZE
Apr 10, 1990K895267ARTECH TYPE SS-HA SUBMERGED SCREW IMPLANT
Artech Corp.
DZE
Dec 21, 1989K891346ARTECH TYPE SS SUBMERGED SCREW IMPLANT
Artech Corp.
DZE
Sep 28, 1989K894160HAND TOOLS FOR ARTECH TYPE SS SUBMERGED SCREW IMPL
Artech Corp.
DZE
Sep 27, 1989K894151IRRIGATED DRILL FOR SS SUBMERGED SCREW PLANT
Artech Corp.
DZJ
Sep 27, 1989K894150COUNTERBORE FOR SS SUBMERGED SCREW PLANT
Artech Corp.
DZJ
Oct 15, 1984K843217HOLLOW BASKET DENTAL IMPLANTS
Artech Corp.
DZE
Sep 27, 1984K843218TPS SCREW DENTAL IMPLANTS
Artech Corp.
DZE

Latest recalls

DateFirm and productCodeLinked 510(k)
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