Clinical & professional resources
Download current public guides for clinical review, evidence evaluation, referrals, DME and coverage planning, training, and responsibly governed pilot discussions.
FDA 510(k) pending. ISO Metrik has not received FDA clearance for the proposed clinical uses described in these materials. Public guides are for professional education and pathway planning.
6 versioned PDF guides
Direct downloads · no form required
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Public download library
Every guide is branded, versioned, dated, and linked to its live pathway. Clinical-use instructions and patient-specific tools remain protected.
A concise orientation to the platform, provider-directed care pathway, supported exercise modes, professional roles, and current evidence and regulatory boundaries.
Eight verified peer-reviewed references with evidence classifications, PubMed and DOI links, and explicit limits on what each source can support.
A provider-to-provider framework for rehabilitation evaluation, secure clinical handoff, care-team roles, privacy, and scope-of-practice boundaries.
A seven-step ordering and supplier-readiness framework covering documentation, coding, coverage, payment, fulfillment, and provider-guided follow-up.
The actual nine-module learning pathway followed by required assessments, practical competency review, authorized sign-off, and certification.
A pre-enrollment framework for research questions, regulatory and IRB determination, protocol design, site readiness, monitoring, and responsible decisions.
Protected clinical library
The Provider & Clinic Portal is the controlled source for current clinical implementation resources. Access depends on role, account status, applicable training, and program authorization.
Screening and fittingCurrent checklists for precautions, inspection, placement, alignment, comfort, and escalation.
Treatment and progressControlled worksheets for parameters, response, comparable measures, and clinical rationale.
Home-program controlsProvider-assigned setup, cleaning, storage, dosage, stopping rules, and clinic contact instructions.
Quality and incident toolsProcesses for product concerns, adverse responses, retraining, corrective action, and required reporting.
Use these materials responsibly
The live pathway pages remain the current public record when a versioned PDF and website content differ.
Pending review does not authorize routine U.S. clinical marketing or use. A clinical investigation must follow the applicable FDA, IRB, IDE, informed-consent, labeling, monitoring, reporting, privacy, and institutional requirements.
The evidence guide classifies every source and states its limitations. No peer-reviewed ISO Metrik-specific clinical outcome publication or public study-registry identifier is currently cited on the public evidence page.
No Medicare DME benefit-category status, dedicated HCPCS Level II code, payer coverage, authorization, allowable amount, or payment is established or guaranteed by these materials.
Do not send patient names, dates of birth, records, images, or other protected health information through public forms, general email, or the website AI assistant. Use an approved secure clinical channel.
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