Start your Manufacturing Journey With Omnee Expo Solutions
At Omnee Expo Solutions, we bridge international buyers with top-tier Indian manufacturers of medical instruments and implants. Our partners are ISO-certified, and we oversee the entire lifecycle — from sourcing and compliance to global export.
We collaborate with a reliable network of ISO 13485-certified third-party manufacturers who specialize in producing high-quality surgical instruments and medical implants. These products are manufactured using various medical-grade materials — including stainless steel, titanium, and polymers — tailored to meet the specific technical and regulatory requirements of each client.
We ensure:
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Manufacturing in ISO-compliant, quality-controlled facilities
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Material selection based on client specifications and application needs
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Adherence to international standards for safety, precision, and performance
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Dimensional and functional testing to ensure consistent quality
Whether you’re sourcing standard catalog items or need custom configurations, our partners deliver precision-engineered products ready for global distribution.
At Omnee Expo Solutions, we ensure that every product delivered by our third-party manufacturing partners adheres to rigorous international quality standards. All instruments and implants undergo thorough quality control procedures at the source, including in-process inspections, dimensional verification, packaging checks, and final batch testing. Our ISO-certified manufacturing partners are required to maintain complete documentation such as batch manufacturing records, material certifications, and sterilization validation (where applicable). We ensure that these partners follow all standard operating procedures (SOPs) and quality protocols in line with ISO 13485 and other applicable regulatory frameworks. Before export, we review the quality documentation and ensure that each shipment is traceable, compliant, and ready for its intended market.
Regulatory compliance is a key pillar of our service offering. We provide clients with comprehensive documentation required for product registration, import clearance, and quality system audits. This includes Certificates of Conformance, ISO 13485 certificates, material test reports, batch records, labeling information, and sterilization certificates where applicable. Our goal is to ensure your products are fully prepared for regulatory scrutiny and ready to meet global compliance standards.
We manage the full export lifecycle, ensuring a seamless and compliant process from order to delivery. Our team coordinates closely with manufacturers and logistics providers to handle production timelines, packing, labeling, and international shipping. We prepare all necessary export documentation, including commercial invoices, packing lists, and airway bills, and liaise with customs agents and freight forwarders to ensure timely clearance and delivery. With a deep understanding of country-specific import requirements, we offer our clients a stress-free experience with full visibility at every stage of the export journey.
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Reliable Manufacturing & Export Solutions for Medical Instruments and Implants