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Symani Post Market Study Shows Trend Toward Reduced Adverse Events and Improved Flap Survival

Home » Timeline Stories » Symani Post Market Study Shows Trend Toward Reduced Adverse Events and Improved Flap Survival

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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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Looking for Symani technical support?

Review Symani Global Indications

Request LVB reimbursement resources

Download Symani Bibliography

Read our latest news

Looking for Symani technical support?

Review Symani Global Indications

Request LVB reimbursement resources

Download Symani Bibliography

Read our latest news

Symani Post Market Study Shows Trend Toward Reduced Adverse Events and Improved Flap Survival

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