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01VEYRA ARC · ROBOTIC-ASSISTED ORTHOPEDICS

Every millimeter, accounted for.

Implants placed within 0.5 mm of plan, on average, in a 412-patient multicenter study.

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REGULATORYCE · FDA 510(k)*
INDICATIONSTKA · UKA · THA
FIRST CASEIn 90 days
FIG. 01 — ARC ARM, LATERALSCALE 1:12
RENDER · ARC ROBOTIC ARM, TECHNICAL LINE DRAWING
0250500 mm
FIG. 02 — EXPLODED VIEWSTEP 1 / 4
PLANNING CONSOLE
ROBOTIC ARM
OPTICAL TRACKER
HAPTIC END-EFFECTOR
Technical line renderings to replace these placeholders
  1. 01 — PLAN

    Plan on the patient’s own anatomy.

    A CT-based 3D model lets the surgeon size and position implants before the day of surgery, with the whole team reviewing the plan together.

    Plan in under 15 min* · DICOM import
  2. 02 — REGISTER

    Register in minutes, not guesswork.

    Optical trackers map the patient’s bone to the plan. Registration is verified before any resection begins.

    330 Hz tracking · sub-mm registration
  3. 03 — EXECUTE

    Stay inside the plan.

    The haptic boundary limits the saw to the planned volume. The surgeon stays in control; ARC keeps them within ±0.5 mm.

    ±0.5 mm haptic boundary
  4. 04 — VERIFY

    Record every case.

    Gap balancing and implant position are logged for each case and exported to your registry through Veyra Connect.

    HL7 FHIR R4 export
02CLINICAL OUTCOMES

Measured, not claimed.

All ARC evidence →
PLACEMENT ACCURACY 0.5mm1 Mean deviation from plan, 412 patients
OR TIME −18%2 Per robotic knee case vs. conventional
LENGTH OF STAY −0.8days3 Across 2,960 patients at 14 sites
¹ VEYRA-01, 2025 · ² St. Aurel Registry, 2025 · ³ VEYRA-02, 2026 · illustrative data. Individual results may vary.
03SPECIFICATIONS
Indications
TKA · UKA · THA
Accuracy (mean)
0.5 mm · 0.5°
Tracking
Optical, 330 Hz
Imaging
CT, DICOM 3.0
Footprint
0.9 × 0.7 m
Weight
248 kg
Power
100–240 V, 50/60 Hz
Setup time
< 12 min
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04INTEGRATION & SERVICE
INTEROPERABILITY HL7 FHIR R4 Case data flows to your EHR and registry. Validated in 38 IT environments.
SECURITY IEC 81001-5-1 Secure development lifecycle, SBOM on request, coordinated disclosure.
SERVICE SLA 4-hour remote response 24/7 line, next-business-day engineer, preventive maintenance included.
TRAINING Surgeon + OR team Certification tracks via Veyra Academy, with proctored first cases.
05ACQUISITION MODELS

Fits your capital cycle.

Model all three in the calculator →
CAPITAL PURCHASE Own the system One-time investment with a multi-year service agreement and software updates included. Best for: > 400 cases / year
OPERATING LEASE Spread the cost Fixed monthly payments over 5–7 years. Off-balance-sheet options in many markets. Best for: budget predictability
PAY-PER-PROCEDURE Pay as you operate No upfront capital. A per-case fee includes disposables, service and training. Best for: new programs, < 250 cases
Availability: Veyra ARC is available in the EU, UK and US.* Hip indications are pending in some markets. Not available in all regions. Notify me for my region
06QUESTIONS

Typically 90 days from agreement: 30 days for installation and IT integration, 30 for team training, then a proctored first case.

See ARC in your OR.

Request a demo → Register for training
A clinical specialist replies within 1 business day · No commitment · Your data stays in the EU
IMPORTANT SAFETY INFORMATION

Indications: Veyra ARC is intended to assist the surgeon in providing software-defined spatial boundaries for orientation and reference information to anatomical structures during total and partial knee and total hip arthroplasty. Rx only. Contraindications include active infection and conditions that prevent CT imaging. Potential risks include those of standard arthroplasty, such as infection, thromboembolism, implant loosening and nerve injury, plus pin-site complications and fracture at tracker sites. Read the full instructions for use before use. Illustrative text.

Indications: Veyra ARC is intended to assist the surgeon in providing software-defined spatial boundaries for orientation and reference information to anatomical structures during total and partial knee and total hip arthroplasty. Rx only. Contraindications include active infection and conditions that prevent CT imaging. Potential risks include those of standard arthroplasty, such as infection, thromboembolism, implant loosening and nerve injury, plus pin-site complications and fracture at tracker sites. Read the full instructions for use before use. Illustrative text.

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