Home » SprintRay Receives FDA’s 510(k) Clearance for Its NightGuard Flex
SprintRay Receives FDA’s 510(k) Clearance for Its NightGuard Flex
SprintRay has received the FDA’s 510(k) clearance for its NightGuard Flex, a dental 3D printed resin, as a Class II medical device.
The resin, which can be used to fabricate orthodontic and dental appliances such as mouthguards, nightguards and splints, enables “uniform, end-to-end dental 3D printing,” the company said.
The FDA defines Class II medical devices as products that present a moderate to high risk to the patient or user.
The Los Angeles, Calif.-based company says it has seen a growing demand for nightguards during the COVID-19 pandemic.
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