Profile: Eyekon Medical specializes in the development of technological advancements of intraocular lenses. We are an ISO 9001 CE MARK certified company. We offer products like hydrophilic acrylic LOLs & disposable injector, natural tinted lens, single PC PMMA LOLs, Viscoelastics, CTR & injector & distribution network The FDA has granted us permission to proceed to phase II clinical trials on their natural clear lens series intraocular lens made of hydrophilic acrylic material, which is a major breakthrough for the ophthalmic industry. Our new material is more biocompatible in the eye compared to conventional hydrophobic lenses presently used and produce sharper vision for patients.
The company was founded in 1987, has revenues of USD 1-5 Million, has ~10 employees and is ISO, CE certified.
FDA Registration Number: 1038833
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• (FDA Code: MSS / 886.4300) An intraocular lens guide is a device intended to be inserted into the eye during surgery to direct the insertion of an intraocular lens and be removed after insertion is completed. |
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• (FDA Code: HQL / 886.3600) An intraocular lens is a device made of materials such as glass or plastic intended to be implanted to replace the natural lens of an eye. |
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• (FDA Code: MFK / 886.3600) |
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• (FDA Code: LZP / 886.4275) An intraocular fluid is a device consisting of a nongaseous fluid intended to be introduced into the eye to aid performance of surgery, such as to maintain anterior chamber depth, preserve tissue integrity, protect tissue from surgical trauma, or function as a tamponade during retinal reattachment. |