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Sutter Medizintechnik GmbH FDA Approvals

0 new drug approvals and 2 device clearances on file. This applicant is not matched to a listed company.

Newest first

A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.

Product
CURIS II RF Generator (REF 360100-05)510(k)Feb 11, 2026General, Plastic Surgery
FlexTip Bipolar electrodes single-use (AR-S9805-0028), FlexTip Bipolar electrodes single-use (AR-S9805-0035)510(k)Jan 25, 2024General, Plastic Surgery

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