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Home » Robotic-Assisted Lymphovenous Anastomosis to Treat Periorbital Lymphedema and Systematic Review of Lymphatic Reconstruction of Face and Neck Lymphedema

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The Symani Surgical System is authorized for use in the U.S. by the FDA and is a CE marked medical device. Symani is manufactured in Pisa, Italy.

Clinical indications vary by geography. Refer to global indications for more information.

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