About GuideMia
We build dental implant software and orthodontic software: the tools that plan guided implant surgery and orthodontic treatment, and design the appliances that deliver it.
- Founded
- Established in southern California, USA, in 2012.
- Offices
- Headquarters in southern California, with a branch office in Shanghai.
- Distribution
- Distributors in Italy, Brazil, China and elsewhere.
- Clearances
- Two FDA 510(k) cleared devices — Implant Master (K121466), the first cleared commercial surgical guide design system, and OrthoPlus (K162850), the first cleared orthodontic software with CBCT integration.
What we build
For more than a decade the focus has not moved: dental implant software for guided surgery, orthodontic software for aligners and brackets, and the open architecture that lets a clinic or a lab use whichever scanner, implant library and printer it already owns.
- GuideMia Implant Master — dental implant software for treatment planning and surgical guide design
- GuideMia OrthoPlus — orthodontic software for planning, clear aligners and bonding guides
- GuideMia OrthoClic — chairside orthodontic software for treatment planning
- CBCT segmentation, run locally on your own machine
- Surgical guides, bracket bonding guides and a universal surgical kit
Regulatory
GuideMia Implant Master is the first FDA cleared commercial surgical guide design system, cleared under K121466. GuideMia OrthoPlus is the first FDA 510(k)-cleared orthodontic software with CBCT integration, cleared under K162850. Both are developed under an ISO 13485 certified quality system. The quality system is certified; the two devices named here are the cleared ones.
GuideMia and Cympha
Cympha is a separate product from a partner company, covering case management and browser-based review. Subscriptions, billing and account support for GuideMia software are handled through Cympha. Cympha itself is not a cleared medical device and GuideMia clearances do not extend to it.