Is customization available?

Yes, we offer flexible customization including minor, full, design-based, and sample-based customization.

What certifications do you have?

We hold CE, ISO, ISO13485:2016, and FDA 510K certifications.

Are you a factory or trading company?

We are a factory in China with 17 years of experience in developing and manufacturing surgical devices.

Non-Surgical Treatment Infant Ear Correction Kits Cryptotia

Name: Non-Surgical Treatment Infant Ear Correction Kits Cryptotia
Brand: Guangzhou T.K Medical Instrument Co., Ltd.
SKU: 2103506375

Guangdong, ChinaGuangzhou T.K Medical Instrument Co., Ltd.

US$165.00-230.00

1 Piece

Sample price:US$200.00/piece.Request sample

Product profile

Customization

Available

Customized

Non-Customized

Certification

ISO, CE

Model NO.

EK-T88L

Condition

New

Tilted

Non-Tilted

Folded

Non-Folding

Using Ambient

Indoor

Using Site

Ear

Power Supply

Manual

Color

White

Material

TPU

Transport Package

Box and Carton Case

Specification

all sizes available

Trademark

Origin

China

Production Capacity

10000 Pieces/Year

Key features

Non-Invasive Correction: Provides a painless, non-invasive solution for infant ear deformities without trauma.

Special Baby Design: Specially designed for babies with soft TPU material for comfortable wearing.

Quick Installation: Easy to handle and install, allowing for complete correction in an outpatient setting.

FDA & CE Certified: Meets world-class quality standards with FDA 510K, CE, and ISO13485:2016 certifications.

Strong R&D Capability: Backed by over 600 applied patents and 20 years of manufacturing experience.

Flexible Customization: Offers full, minor, and design-based customization options for OEM/ODM needs.

Global Export Experience: Exported to over 40 countries in America and Europe with successful factory audits.

100% Quality Inspection: Every product undergoes strict functional and visual inspection before shipment.

Company profile

Importers and ExportersHigh Repeat Buyers ChoiceCooperated with Fortune 500Years of Export Experience

Guangzhou T.K Medical Instrument Co., Ltd.

Guangdong, China

CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service Available CertifiedCustomization Options: Customization from Samples, Customization from Designs, etc. CertifiedExport Year: 21 Years CertifiedNearest Port: Guangzhou Port, Shenzhen PortAverage Response Time: ≤3.98h

AI-Powered supplier vetting

SummaryThe supplier is a medical-device manufacturer with 17 years of stated development and manufacturing experience, 17 years of R&D engineer experience, nine production lines, and 21–30 quality-control staff. It reports CE marking for all GTK Medical products and sales to more than 40 countries, including the United States, Germany, the United Kingdom, France, Italy, Spain, Belgium, Japan, and South Korea. The supplier holds or reports ISO45001:2018, ISO14001, CE, and RoHS-related certifications or capabilities. Its R&D profile includes recent new-product development, more than 600 patent applications, more than 200 granted patents, 3D design, ODM, OEM, SDK, and multiple customization services. Service procedures, corrective-action processes, and complaint-handling records are reported. Limitations include no valid manufacturing-capacity contract with related subcontractors, no overseas warehouse or showroom, and no stated overseas-service country coverage despite reporting overseas agents or branches....

Supplier typeThe supplier is identified as a hi-tech medical-device company focused on development and manufacturing, with 17 years of stated experience. Its product description and medical-device R&D positioning support classification as a medical-device manufacturer rather than a general trading or service company.

CertificationsThe supplier states that all GTK Medical products are CE marked and reports CE and RoHS product-certification capability. It also lists ISO45001:2018 and ISO14001 under sustainable-development management certifications; however, the supplier-management-system certification field is only recorded as “Others,” so the full certification scope is not completely specified.

After-Sales capabilityThe supplier reports written and followed procedures for service assessment, corrective and preventive actions, and customer complaints, along with inventory capability and service through overseas agents or branches. It also reports participation in MEDICA, CES, and WHX DUBAI, but has no overseas warehouse or showroom and states zero countries for overseas services, creating a limitation in documented international service coverage.

R&D capabilityThe supplier reports 17 years of R&D engineer experience, new products during the past year, available SDK capability, ODM and OEM services, and more than 600 patent applications including more than 200 granted patents. These are explicit indicators of established product-development and innovation capability.

Production capacityThe supplier operates nine production lines and has 21–30 quality-control staff, while also reporting in-stock capability and average peak- and off-season lead times of within 15 workdays to one month. Nevertheless, it states that neither the factory nor related subcontractors have a valid manufacturing-capacity contract, which is a documented production-governance weakness.

Customization capabilityThe supplier provides 3D software design services and supports flexible, minor, full, design-based, and sample-based customization. Its reported ODM, OEM, and SDK capabilities further support the ability to adapt or develop products for customer requirements.

Client casesThe supplier states that its products are sold in more than 40 countries, including multiple developed markets, and reports OEM service for well-known brands. Participation in MEDICA, CES, and WHX DUBAI provides additional evidence of market-facing activity, although no specific customer names or individually verifiable case details are supplied.