Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Artech Corp. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Mar 5, 1992: ARTECH ARDENT IV - TYPE CLYLINDER IMPLANT.
| Mar 5, 1992 | ARTECH ARDENT IV - TYPE CLYLINDER IMPLANTK911735 · DZE | 510(k) clearances |
| Apr 10, 1990 | ARTECH TYPE SS-HA SUBMERGED SCREW IMPLANTK895267 · DZE | 510(k) clearances |
| Dec 21, 1989 | ARTECH TYPE SS SUBMERGED SCREW IMPLANTK891346 · DZE | 510(k) clearances |
| Sep 28, 1989 | HAND TOOLS FOR ARTECH TYPE SS SUBMERGED SCREW IMPLK894160 · DZE | 510(k) clearances |
| Sep 27, 1989 | COUNTERBORE FOR SS SUBMERGED SCREW PLANTK894150 · DZJ | 510(k) clearances |
| Sep 27, 1989 | IRRIGATED DRILL FOR SS SUBMERGED SCREW PLANTK894151 · DZJ | 510(k) clearances |
| Oct 15, 1984 | HOLLOW BASKET DENTAL IMPLANTSK843217 · DZE | 510(k) clearances |
| Sep 27, 1984 | TPS SCREW DENTAL IMPLANTSK843218 · DZE | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
