Not currently registered with FDA under this name
Artech Corp.
Chantilly, VA, United States. Named as applicant on 8 dental 510(k) clearances between 1984 and 1992. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 81984–1992
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 1980–2026
510(k) clearances
Clearances on which FDA names Artech Corp. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 5 Mar 1992 | K911735 | ARTECH ARDENT IV - TYPE CLYLINDER IMPLANT | DZE Root-Form Endosseous Implant |
| 10 Apr 1990 | K895267 | ARTECH TYPE SS-HA SUBMERGED SCREW IMPLANT | DZE Root-Form Endosseous Implant |
| 21 Dec 1989 | K891346 | ARTECH TYPE SS SUBMERGED SCREW IMPLANT | DZE Root-Form Endosseous Implant |
| 28 Sep 1989 | K894160 | HAND TOOLS FOR ARTECH TYPE SS SUBMERGED SCREW IMPL | DZE Root-Form Endosseous Implant |
| 27 Sep 1989 | K894151 | IRRIGATED DRILL FOR SS SUBMERGED SCREW PLANT | DZJ Manual Wire Driver and Bone Drill |
| 27 Sep 1989 | K894150 | COUNTERBORE FOR SS SUBMERGED SCREW PLANT | DZJ Manual Wire Driver and Bone Drill |
| 15 Oct 1984 | K843217 | HOLLOW BASKET DENTAL IMPLANTS | DZE Root-Form Endosseous Implant |
| 27 Sep 1984 | K843218 | TPS SCREW DENTAL IMPLANTS | DZE Root-Form Endosseous Implant |
Sources
FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.