- ISO 13485 management system
- FDA compliant quality records system
- Environmentally controlled warehouse
- Sustains current good manufacturing practices required for regulatory compliance
- Monitoring, diagnostic, and therapeutic devices
- Specialized in Class II medical devices
- Utilize conductive inks and medically approved substrates
- Completely sealed designs
- Ability to develop product test plans specific to customer requirements (including functional and continuity tests)
- Flexible manufacturing
- Equipment and tool development
- High volume manufacturing
- Cellular manufacturing
- Custom automation & semi automation
