Artech Corp.
Artech Corp. holds FDA 510(k) medical device clearances, first cleared 1984, most recent 1992.
Top product codes for Artech Corp.
Recent clearances by Artech Corp.
- K911735 — ARTECH ARDENT IV - TYPE CLYLINDER IMPLANT
- K895267 — ARTECH TYPE SS-HA SUBMERGED SCREW IMPLANT
- K891346 — ARTECH TYPE SS SUBMERGED SCREW IMPLANT
- K894160 — HAND TOOLS FOR ARTECH TYPE SS SUBMERGED SCREW IMPL
- K894150 — COUNTERBORE FOR SS SUBMERGED SCREW PLANT
- K894151 — IRRIGATED DRILL FOR SS SUBMERGED SCREW PLANT
- K843217 — HOLLOW BASKET DENTAL IMPLANTS
- K843218 — TPS SCREW DENTAL IMPLANTS
Data sourced from openFDA. This site is unofficial and independent of the FDA.