ZettaYotta

ZettaYotta, founded in 2020 as a division of ProKSys LLC, specializes in healthcare interoperability solutions and cloud-native healthcare technology. The company focuses on SMART on FHIR applications, data integration, and standards-based healthcare communication including HL7 v2.x, 3.0, FHIR, and X12 EDI.

The company offers a suite of cloud-deployable products designed for AWS and Azure environments, including zyEMPI (enterprise master patient index), zyFirefly (FHIR server), zyHEngine (HL7 interface engine), zyXEngine (X12 interface engine), zyGhost (AI-powered PHI de-identification), and zySCORE (quality scoring for regulatory compliance). All products are deployed via Terraform automation and can be customized through their marketplace.

ZettaYotta emphasizes adherence to FDA guidelines for Software as a Medical Device development and positions itself as adaptable to client methodologies, whether Agile or traditional SDLC. The company serves providers, payers, and healthcare technology startups with a focus on interoperability and cloud-based solutions.

Choose ZettaYotta if you need modern, cloud-native interoperability solutions with strong standards adherence and the flexibility to deploy in your own cloud infrastructure. Their approach is particularly relevant for organizations transitioning to FHIR-based architectures or building custom healthcare applications that require robust interface engines.

The company's emphasis on FDA SaMD compliance and modular architecture makes them suitable for healthcare technology companies developing regulated medical software, as well as established healthcare organizations modernizing their integration infrastructure with infrastructure-as-code practices.

ZettaYotta is exclusively focused on healthcare technology, with particular expertise in providers, payers, revenue cycle management, and medical devices. Their product suite addresses core healthcare IT challenges including patient identity management (EMPI), clinical data exchange (FHIR/HL7), claims processing (X12 EDI), and PHI security. The company's adherence to FDA guidelines for Software as a Medical Device demonstrates commitment to healthcare regulatory requirements.

Their interoperability solutions support multiple healthcare standards essential for modern care coordination, including SMART on FHIR for application integration, C-CDA for clinical document exchange, and both 837/835 transactions for claims processing and 270/271 for eligibility verification.

Mid-sized healthcare organizations or health tech startups with cloud infrastructure expertise who need standards-based interoperability solutions. Organizations seeking to maintain control over their infrastructure while leveraging pre-built, modular components for FHIR, HL7, and EDI integration. Those developing Software as a Medical Device who value FDA compliance expertise.