I.See Vision Technology Inc.

SUPPLIER PROFILE: I.See Vision Technology Inc. I.See Vision Technology Inc. is a manufacturer of eyewear and accessories based in Hsinchu County, Taiwan. The company was founded in 1999 and operates with a workforce in the 201-500 employee range. PRODUCTS AND FOCUS I.See Vision Technology specializes in eyewear and related accessories. The company serves the eyewear sector, which encompasses both corrective and protective eyewear applications. Specific product lines, manufacturing capabilities, and technical specifications are not available in current public records. MARKET PRESENCE I.See Vision Technology exports to a broad geographic footprint spanning multiple regions: Central and South America, Chinese Mainland, Eastern Europe, Hong Kong, Japan, the Middle East, other Asian countries, Scandinavia, Southeast Asia, Taiwan, and Western Europe. This distribution pattern indicates established supply relationships across developed and developing markets. CERTIFICATIONS AND COMPLIANCE The company holds multiple quality and regulatory certifications relevant to eyewear manufacturing: - CE Mark and CE 0434 certification, indicating compliance with European Union medical device directives where applicable - ISO 13485 certification, the international standard for medical device quality management systems - GMP (Good Manufacturing Practice) certification, demonstrating adherence to pharmaceutical and medical device manufacturing standards - Additional ISO certifications (specific standards not detailed in available records) These certifications suggest the company manufactures medical-grade or regulated eyewear products and maintains formal quality management systems. BUSINESS STRUCTURE As a manufacturer rather than a trader or distributor, I.See Vision Technology likely handles production in-house or through controlled partnerships. The Taiwan-based location provides access to the region's established eyewear manufacturing ecosystem and supply chain infrastructure. CREDIBILITY SIGNALS The company's 25-year operating history (founded 1999), multi-regional export presence, and portfolio of medical device certifications provide foundational credibility signals. The combination of CE Mark and ISO 13485 compliance suggests experience navigating regulated markets and international quality requirements. INFORMATION GAPS A company website is not currently available in public records, which limits direct verification of current product offerings, technical specifications, and manufacturing capacity. Trade fair participation records are not documented. Harmonized System (HS) codes are not listed, preventing tariff classification analysis. Current management structure, facility details, and recent business development information are not available. NEXT STEPS FOR BUYERS Interested buyers should conduct direct outreach to verify current product portfolios, manufacturing capacity, lead times, and pricing. Request documentation of certifications, quality audits, and references from existing customers in relevant markets. Confirm export compliance procedures and any restrictions on product categories or regions.