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Oculus receives 510(k) clearance for Pentacam AXL
The Pentacam AXL has received 510(k) clearance from the FDA, Oculus announced in a press release.The device, which combines anterior segment tomography and optical biometry for premium IOL calculation, integrates standard IOL formulas and ray-tracing formulas. Toric IOL calculation is based on total corneal refractive power and factors in the posterior corneal surface, the release said.