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LensAR laser system gains 510(k) clearance for arcuate incisions
The LensAR laser platform has received 510(k) clearance from the U.S. Food and Drug Administration for the creation of arcuate incisions during cataract surgery, according to a company news release.The device may now be used during cataract surgery for corneal and arcuate incisions, lens fragmentation and anterior capsulotomy with or without phacofragmentation, the release said.