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Erchonia s Low-Level Laser Receives Market Clearance for Whole-Body Postop Pain

Erchonia has received 510(k) clearance from the US Food and Drug Administration for its low level laser technology to treat whole-body postoperative pain.

Travis sammonsWorld leader in low level laser technologyDrug administrationErchonia clinical affairsWorld leaderLow level laser technologyClinical affairs manager

FDA Grants 510(k) Market Clearance for Whole Body Postoperative Pain to World Leader in Low Level Laser Technology

Melbourne, FL (PRWEB) November 01, 2021 Erchonia, the World Leader in Low Level laser Technology announces that on October 22, 2021, they have received

Travis sammonsWorld leader in low level laser technologyErchonia clinical affairsWorld leaderLow level laser technologyLow levelGlobal postoperative pain management marketClinical affairs managerPress release

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