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Orthopedic Spinal Implants Instrument Intervention Materials Lumbar Titanium Cage
US$72.60
1-99 Pieces
US$70.00
100+ Pieces
Sample price:US$72.60/piece.Request sample

Product profile

Customization

Available

Type

Trauma Plate

Application

Orthopedic

Model NO.

714

Material

Titanium

Feature

Disposable

Certification

CE, ISO13485

Group

Adult

Usage

Bone Fracture Fixation

MOQ

1 PC

Color

Grey

Surface(Ti)

Micro-Arc Oxidation

Shipping

DHL\UPS\FedEx\EMS\TNT Air Cargo

OEM/ODM

Accept

Transport Package

PE Bags, One Inner Carton and One Outer Carton.

Specification

8*20-14*26mm

Trademark

Jinlu

Origin

Jiangsu, China

HS Code

9021100000

Production Capacity

1000PCS/Month

Key features

CE & ISO13485 Certified: Products meet EU CE standards and ISO13485 quality system certification.
Titanium Alloy Material: Made from high-quality Titanium Alloy with Micro-Arc Oxidation surface treatment.
Full Customization Available: Supports customization from samples, designs, and flexible minor adjustments.
Low MOQ Requirement: Minimum Order Quantity is just 1 PC, suitable for trial orders.
100% Quality Inspection: Strict QA/QC with 4 inspectors performing 100% visual inspection on finished products.
Established Manufacturer: Jiangsu Jinlu Group established in 1958 with over 57 years of industry experience.
Fast Lead Time: Average lead time within 15 workdays for both peak and off-season periods.
Traceable Raw Materials: Full traceability of raw materials ensures product authenticity and quality.

Company profile

Jiangsu Jinlu Group Medical Device Co., Ltd.
High Repeat Buyers ChoiceYears of Export ExperiencePatents AwardedExhibition Experience
CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available CertifiedCustomization Options: Customization from Samples, Customization from Designs, etc. CertifiedExport Year: 15 Years CertifiedNearest Port: Shanghai PortAverage Response Time: ≤4.56h

AI-Powered supplier vetting

SummaryThe supplier is a combined company engaged in manufacturing, processing, sales, and import/export of medical devices, with additional non-medical mask activities. It demonstrates broad customization and R&D/ODM capabilities, reports new products within the past year, and has documented inspection, supplier assessment, corrective-action, and complaint-handling procedures. Export experience is established, with 15 years of exporting and 41%–50% of total sales from exports. Service infrastructure is limited: it reports no overseas warehouses, showrooms, agents, or branches, although it has participated in the CMEF offline trade show. Financial information is insufficient for assessing credibility. The provided information does not establish certifications, customer cases, or internationally recognized design awards. Digital sustainability capabilities are also limited, including no ERP-based process integration.
Supplier typeThe supplier is identified as a combined company whose scope includes medical-device manufacturing, processing, sales, and import/export, plus production and sales of non-medical daily masks. Its declared offering covers manufacturing, export trade, service, quality control, R&D, and sustainable-development capabilities.
After-Sales capabilityThe supplier states that it has clear, followed procedures and records for customer complaints, corrective and preventive actions, and supplier-service assessment, and describes complete after-sales service as a corporate objective. However, it has no overseas warehouse, showroom, agent, or branch; therefore, documented complaint handling exists, but overseas service coverage is limited.
R&D capabilityThe supplier reports R&D capability, at least one new product within the past year, ODM services, and a development focus on science, technology, and innovative technology. Nevertheless, it reports no internationally recognized design awards and no available SDK, so the evidence supports operational product development but not broad external innovation recognition.
Production capacityThe supplier’s business scope explicitly includes medical-device manufacturing and processing. It reports uniformly followed finished-product inspection instructions, written and followed service-assessment procedures, corrective-action records, complaint-handling records, and lead times within 15 workdays in both peak and off-season; these indicate established production and quality-process capability.
Customization capabilityThe supplier explicitly offers customization from samples, customization from designs, full customization, minor customization, and flexible customization. It also reports R&D capability and ODM service availability, providing direct evidence of broad customization support.

Product Q&A

Q:What certifications do the implants have?
A:
Our products are certified with CE and ISO13485, meeting EU standards and quality system requirements.
Q:What is the minimum order quantity?
A:
The Minimum Order Quantity (MOQ) is 1 PC, allowing for flexible purchasing options.
Q:Can the products be customized?
A:
Yes, we offer full customization including from samples, designs, and flexible minor customization options.
Q:What is the production lead time?
A:
The average lead time is within 15 workdays, applicable to both peak and off-season periods.
Q:How do you guarantee product quality?
A:
We conduct 100% visual inspection on finished products, use traceable raw materials, and perform pre-production samples and final inspections.

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