The LightMed Corporation is an international company with its foundations in the Medical Instrumentation manufacturing field. With over 15 years experience in this field and in drawing its expertise from many countries, including the USA and
Australia, we have ambitious plans and goals for the future.
LightMed is a designer, manufacturer and distributor of Ophthalmic Medical Equipment with our main focus for the future being Laser treatment products.
Our personnel have a wealth of experience in the Medical Equipment industry in the Laser, Optical, Electronic and Mechanical areas. With our close affiliations to many of the Universities, Hospitals and Scientific research centers in Taiwan we are also able to work together with these organizations to further enhance our own knowledge base and thereby develop new technologies and produce better products.
Our head office is in Taipei, Taiwan primarily because of the close ties to these organizations and the Hi-tech industry that exists here, which enables ready access to quality, low cost materials for our manufacturing. These cost savings can be passed on to our customers with lower cost products.
We also have an office in California
LightMed(USA),INC. and through our International distributors we have worldwide coverage.
The LightMed mission is to design, manufacture and sell excellent quality products that meet our customers requirements. We require our products to give good reliable service for their working life and we offer a strong customer service backup in support of this.
Our Quality Management System ensures that we maintain a consistent and controlled work environment for all aspects of the company to our established internal procedures. This then also ensures that our products always meet the specifications and requirements of the various Regulatory authorities throughout the world
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Being an International Company we are committed to a Quality System that encompasses the requirements of many countries and systems including:
- European ISO 13485：2003 Quality System for Medical Devices- USA FDA Current Good Manufacturing Practices
- European CE Mark (MDD 93/42/EEC) for Medical Devices.
- Taiwan (ROC) Medical Device GMP
- Chinese SPAC (PRC) Medical Device Registration provisions
- Other Registration requirements of various countries
The LightMed Quality System has been certified to the ISO13485：2003, MDD and GMP requirements and our products carry the CE Mark according to the MDD. LightMed is a registered manufacturing Establishment with the FDA and our products have 510(k) approvals and are Listed Devices with the FDA.
LightMed plans to consolidate its presence in the Ophthalmic Industry but will continue to look for opportunities in whatever field they may be in so we can use our technical, manufacturing and marketing expertise to its greatest potential.
By providing good service and co-operation with our customers and distributors we believe there will be a bright and rewarding future for all.
We look forward to serving you and please " Contact us " if you require any additional information.
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| QC inspection using Precision measuring instrumentation on all parts |
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| All products and sub-assemblies are 100% tested for function and performance to specifications |
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| All electronic and mechanical assembly is performed in-house and under strict Quality Control |
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| We utilise all the latest in technologies in optical Laser systems and assemble in controlled conditions |
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