About Icare
Icare is building a connected, cybersecure, evidence-anchored platform across patient monitoring, dental practice systems, and laboratory diagnostics.
Software Bill of Materials disclosed for every connected Class II monitoring and IVD device, with design history file (DHF) change linkage.
Native bidirectional exchange with Epic, Cerner, and MEDITECH for RPM and LIS workflows.
Class IIb ML alarm-assist models update under FDA Predetermined Change Control Plans.
Dental CBCT and chemistry analyzers complete software commissioning without on-site engineers.
Net-zero Scope 1+2 operations and published LCA packs for the full active SKU set then under contract.
First multi-parameter monitor with published SpO2 accuracy envelope
Dental CAD/CAM chairside line cleared for DSO rollouts
Remote patient monitoring kit with FHIR Observation push
Full IVD chemistry/hematology stack CE marked under IVDR
Unified Spec Library with UDI-DI bulk export
Anonymous facility-type references — hospital names are not published without written authorization.
Icare does not claim universal clinical superiority. Pulse oximetry SpO2 accuracy envelopes assume adequate perfusion; wearable RPM kits are validated for typically 8 hours continuous monitoring; analyzer coefficient of variation (CV) and limit of detection (LOD) remain assay-lot dependent; and dental CBCT requires confirmed DICOM interoperability with your picture archiving and communication system (PACS) or vendor-neutral archive. Where value-analysis committees debate single-use device (SUD) trays versus reusable instruments, we publish autoclave / steam sterilization and ethylene oxide sterilization cycle limits rather than prescribe a single pathway.