# Artech Corp.

- Location (FDA's records): Chantilly, VA
- FDA decisions: 8 (1984–1992): 8 510(k) clearances
- Product codes: DZE (6), DZJ (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 6 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Crystal Medical Technology: 2 (https://510kreport.com/company/crystal-medical-technology)
- Quantum Bioengineering, Ltd.: 2 (https://510kreport.com/company/quantum-bioengineering)
- Dentatus USA, Ltd.: 2 (https://510kreport.com/company/dentatus-usa)

## Its most-cited devices
- K891346: Artech Type SS Submerged Screw Implant (1989), cited by 3
- K895267: Artech Type SS-HA Submerged Screw Implant (1990), cited by 3

## Recent decisions
- K911735: Artech Ardent IV - Type Clylinder Implant (Mar 5, 1992)
- K895267: Artech Type SS-HA Submerged Screw Implant (Apr 10, 1990)
- K891346: Artech Type SS Submerged Screw Implant (Dec 21, 1989)
- K894160: Hand Tools for Artech Type SS Submerged Screw Impl (Sep 28, 1989)
- K894151: Irrigated Drill for SS Submerged Screw Plant (Sep 27, 1989)
- K894150: Counterbore for SS Submerged Screw Plant (Sep 27, 1989)
- K843217: Hollow Basket Dental Implants (Oct 15, 1984)
- K843218: TPS Screw Dental Implants (Sep 27, 1984)

Source page: https://510kreport.com/company/artech