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High Quality Pure Titanium Orthopedic Implants Distal Fibular Locking Compression Plate I with CE Certificate
US$44.00
1-99 Pieces
US$41.00
100+ Pieces
Sample price:US$44.00/piece.Request sample

Product profile

Customization

Available

Application

Orthopedic

Certification

CE, ISO13485

Model NO.

262

Color

Grey Color/Shine

Size

3-10 Holes

Brand

Jinlu /OEM

Certificate

CE,FDA,ISO

Model Number

262

Package

PE Bag Orders in Carton

Usage

Bone Fracture Orthopedic

Transportation

DHL/TNT/EMS/UPS/FedEx/Air

Payment

30% for Advance Order

Relating Items

Screw and Instruments

Transport Package

PE Bag for Each Pieces,

Specification

CE ISO certificate

Trademark

JINLU/OEM

Origin

Zhangjiagang, Jiangsu

HS Code

9021100000

Production Capacity

10000 PCS/Month

Key features

CE & ISO Certified: Products certified with CE, ISO13485, and FDA standards for safety and quality.
Customizable Options: Offers customization in color, size, brand, and design based on samples or drawings.
Established Manufacturer: Jiangsu Jinlu Group, established in 1958, with 57 years of R&D and manufacturing experience.
Strict Quality Control: 100% visual inspection, pre-production samples, and final checks before shipment.
Wide Application Range: Suitable for orthopedic bone fractures with various hole sizes from 3 to 10.
Flexible Payment Terms: Accepts USD, EUR, CNY via T/T, L/C, Western Union, Cash, or Escrow.
Global Logistics Support: Ships via DHL, TNT, EMS, UPS, FedEx, or Air freight with FOB/CIF/EXW terms.

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: ≤4.05h

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 is the material of the distal fibular locking plate?
A:
The plate is made of pure titanium, ensuring high quality and biocompatibility for orthopedic implants.
Q:What certifications does the product have?
A:
The product holds CE, ISO13485, and FDA certifications, meeting strict international medical standards.
Q:Is customization available for this implant?
A:
Yes, we offer customization for color, size, brand, and design, including full and minor customization options.
Q:What is the minimum order quantity?
A:
The minimum order quantity is 1 piece, allowing for flexible purchasing for various needs.
Q:What is the lead time for production?
A:
The average lead time is within 15 workdays for both peak and off-season periods.

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