IMETRIC ICam Full-Arch Implementation Checklist
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Implementation checklist
Installing ICam is not the same as implementing it. Production readiness requires the correct bundle, accessories, validated component protocol, calibration, reprocessing, secure file handoff, laboratory acceptance, and a trained backup operator.
Build the workflow around a written case path before the first definitive patient. That path should make failure visible early, while the patient and capture components are still available.

Inventory the complete system
Confirm the ICam unit, computer and software requirements, calibration plate, ICamBodies, screws, cables, carrying case contents, reprocessing supplies, and spare strategy. Record serial numbers and accessory quantities.
The IMETRIC accessory policy makes careful unboxing important. Remove and account for all contents and packing materials before discarding the shipping materials, then store precision components in assigned locations.
Write the chairside sequence
Define patient and case verification, component selection, seating checks, calibration, capture order, quality review, repeat criteria, decontamination, and documentation. Include what the user does when the system or software reports a problem.
Train with the exact components and restorative workflow used in production. Generic demonstrations are not enough when connection, screw, and data-path details determine the result.
Validate the laboratory path
Agree on required files, naming, transfer method, software import, positional-data format, companion IOS scans, bite records, photos, and prescriptions. Send test records through the real secure channel.
The laboratory should confirm receipt, correct assignment, successful import, and registration before the workflow is considered live. Keep software and protocol versions with the validation record.
Monitor outcomes
Track calibration failures, repeat captures, component problems, file-transfer issues, registration questions, verification outcomes, fit adjustments, remakes, and operator. Review early cases as a team.
Implementation is complete only when a second trained user can run the workflow and the laboratory can identify and reject an incomplete submission before design.
Related Dentcore guides
Product capabilities, indications, validated materials, software support, and regulatory availability can change. Confirm the current manufacturer documentation and case requirements before purchase or clinical use. Dentcore can help review the configuration, but the treating clinician and laboratory remain responsible for case selection and the validated workflow.