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Patient-specific surgical guide manufacturing

From approved digital plan to manufactured guide.

Invivo Guide™ patient-specific surgical guides are produced from dental professional-approved case information through digital planning, controlled manufacturing, and documented final inspection.

✓ Prescription-based case requirements✓ Final fabrication and inspection in Santa Clara
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Single- and multi-siteCase-dependent availability
Guide configurationsConfirmed during case review

A documented case workflow

Case information, approval, manufacturing, and final inspection.

Each accepted case follows defined steps based on the dental professional’s prescription and approved case specifications.

Approved case information

Manufacturing begins after the required prescription, case records, and guide design approval are received from the dental professional.

Defined digital workflow

Case information moves through documented review, design approval, manufacturing, and final release steps.

Case-specific guide options

Guide material and configuration are confirmed for each accepted case based on current service information and case requirements.

Documented final inspection

Final fabrication and inspection activities are performed and documented at D-CUBE’s Santa Clara facility.

Defined workflow

A clear path for each accepted case.

Required case records, design approval, manufacturing, and final inspection are handled through defined steps.

01

Submit

Provide the prescription and required case records through the designated secure workflow.

02

Approve

The dental professional reviews and approves the guide design before manufacturing.

03

Manufacture

The guide is produced to the approved case specifications under documented work instructions.

04

Inspect

Final fabrication and inspection are completed and documented before release.

Case-specific compatibility review

Confirm the system before case acceptance.

Guide configuration and component compatibility depend on the implant system, guided kit, case records, and current service availability. D-CUBE confirms compatibility for each submitted case before manufacturing.

  • ✓ Implant system and guided kit identified
  • ✓ Required case records reviewed
  • ✓ Compatibility confirmed before acceptance
Systems referenced in current workflowVerify by case
✓ Nobel✓ Biomet 3i✓ Straumann✓ BioHorizons✓ Zimmer✓ Camlog✓ Implant Direct✓ Astra Facilitate✓ Neoss✓ ZimVie

System names identify compatibility-review categories only. Availability is case-specific and is not guaranteed.

Controlled manufacturing

Final fabrication and inspection in Santa Clara.

Invivo Guide final fabrication and documented inspection are performed by D CUBE, Inc. at 3350 Scott Blvd., Building 29, Santa Clara, CA 95054 USA.

For licensed dental professionals. The treating dental professional is responsible for diagnosis, treatment planning, the prescription, design approval, clinical verification, and use of the guide. Review current product information and applicable instructions for use. View Invivo Guide product information →

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