Q&A: Fiber-Optic Technology Meets Dental Science
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Q&A: Fiber-Optic Technology Meets Dental Science

Q&A: Fiber-Optic Technology Meets Dental Science

john tokizawa qa,Q: Can you talk about why you formed iLumi Science?, ,A: I worked for nearly 3 decades for a manufacturer that primarily dealt with military night vision components such as microchannel plates, faceplates, and inverters. One day, a dentist visited me with a request to produce a fi ber post with the two most desired characteristics—light transmission and radiopacity, but without compromising either feature. I formed iLumi Sciences in Chantilly, VA, in 2011. After 3 years of research and development, iLumi achieved a perfect balance of unmatched light transmission and more than 5x radiopacity with the Super Fiber Post. We collaborate with dentists worldwide, listen to their needs, and focus on improving dental products. We seek to present innovative and intelligent solutions that dentists will appreciate. All of our products are made in the United States, and we have strengthened our customer support with an in-house service team and a toll-free number. Customers can get fast delivery and answers to all their questions very quickly, , ,Q: Is there collaboration between fi ber-optic specialists and dental professionals?, ,A: Yes, the development of the Super Fiber Post started with fiber-optic masters and dentists, and we work closely with dentists for new product development projects., , ,Q: How does the Super Fiber Post achieve 5x radiopacity, and what are the key benefi ts of this feature?, ,A: The radiopacity level is achieved through the optical properties and composition, for which iLumi holds the patent. Radiopacity is essential for ease and detailed x-ray visibility when the posts are surrounded by tooth, bone tissue, and core material., ,Q: Can you give us a peek inside the iLumi facility in Virginia and the process for testing and approving products?, ,A: Our employees are dedicated and detail-oriented. The inspection procedures, tests, and product approval make up a tedious process based on good manufacturing practices and ISO 13485:2016, as well as a complete technical construction fi le required by CE. There is a process of detailed design and development of the product—everything from scientific studies and reports to detailed lot inspections. Constant post-market surveillance    is conducted, and various publications support the integrity and sale of the product., , 

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