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Titanium 5.5 Polyaxial Screw System for Minimally Invasive Surgery with ISO
US$75.00
1-4 Pieces
US$72.00
5-9 Pieces
US$69.00
10+ Pieces

Product profile

Type

5.5 Mis Spinal System II

Syringe

5.5 Mis Spinal System II

Blood Sampling Needle

5.5 Mis Spinal System II

Model NO.

5.5 MIS Spinal System II

Breathing Pattern

5.5 Mis Spinal System II

Animal Anesthesia Machine Control Method

5.5 Mis Spinal System II

Certification

FDA, CE

Disinfection

Disinfection

Color

5.5 Mis Spinal System II

Application

5.5 Mis Spinal System II

Material

Titanium

Transport Package

PE Film

Specification

1pcs

Trademark

XC MEDICO

Origin

China

Key features

Minimally Invasive Design: Small incision approach ensures minimal bleeding and fast postoperative recovery.
Anti-Loosening Fixation: Cement augmentation provides strong fixation in osteoporotic bone, reducing loosening risk.
High-Strength Titanium Alloy: Made from qualified TC4 titanium alloy with excellent mechanical properties and traceability.
Versatile Clinical Indications: Suitable for thoracolumbar fractures, degenerative conditions, tumors, and revision procedures.
FDA & CE Certified: Products meet international safety standards with FDA and CE certifications.
Customization Available: Minor customization options available for specific clinical needs and branding.
Comprehensive System: Includes screws, rods, and compression-distraction forceps for complete spinal correction.

Company profile

Xc Technology Co., Ltd.
In-stock CapacityFast DeliveryRaw-Materials TraceabilityQuality Assurance
CertifiedBusiness Type: Trading Company CertifiedCustomization Options: Minor Customization CertifiedExport Year: 6 Years CertifiedNearest Port: Shanghai PortAverage Response Time: ≤6.62h CertifiedTerms of Payment: LC, T/T, D/P, etc.

AI-Powered supplier vetting

SummaryXC Medico is identified as a trading company serving the health and medicine sector, with orthopedic instruments as a key product area. The supplier reports 18 years of orthopedic experience, certified production lines and warehouses, raw-material traceability, and 100% finished-product inspection, although inspection is performed by packing staff and only one quality inspector is reported. Service infrastructure is limited: no overseas warehouses, showrooms, agents or branches, and no offline trade-show participation. Formal service procedures, corrective/preventive-action records, and complaint-handling procedures are not provided. Innovation evidence is weak, with no new products in the past year, no ODM, OEM for popular brands, or SDK. Minor customization is available. Certification is mentioned, but specific certificates are not identified. Customer cases are not documented.
After-Sales capabilityThe supplier claims technical support covering preoperative planning, intraoperative assistance, and postoperative traceability and complication management. Against this, it reports no written service procedures or records, no formal corrective/preventive-action mechanism, no documented complaint-handling process, and no overseas warehouses, showrooms, agents or branches; therefore, structured and geographically accessible after-sales capability is not demonstrated.
R&D capabilityThe supplier describes experienced engineers and product development and innovation, but reports no new products during the past year, no ODM service, no OEM for popular brands, and no available SDK. The explicit recent innovation and development offerings therefore indicate a deficiency.
Production capacityThe supplier states that it operates certified production lines and warehouses, has a 668.0 m² manufacturing plant, provides raw-material traceability, and conducts 100% finished-product inspection. However, finished products are checked by packing staff and only one quality inspector is reported; production capability is supported by facility and control claims, but its scale and robustness are only partially evidenced.
Customization capabilityThe supplier explicitly offers minor customization. This confirms some customization capability, but the evidence does not show advanced engineering customization, extensive configuration options, or full OEM/ODM support.

Product Q&A

Q:What are the main advantages of this minimally invasive system?
A:
It offers minimal bleeding, fast recovery, anti-loosening fixation via cement augmentation, and controllable fluoroscopy-guided accuracy with low leakage risk.
Q:What materials are used for the screws and instruments?
A:
All products use qualified TC4 titanium alloy conforming to GB/T 13810-2017, ensuring excellent mechanical properties and biocompatibility.
Q:What clinical indications are supported by this system?
A:
It is indicated for thoracolumbar osteoporotic fractures, degenerative conditions, spinal tumors, and revision procedures involving implant failure or instability.
Q:Is customization available for this product?
A:
Yes, minor customization options are available. Please contact us for full catalog to customize sets or specific designs.
Q:What certifications does the product hold?
A:
The product holds FDA and CE certifications, ensuring compliance with international medical device standards.

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