Sutter Medizintechnik GmbH - FDA 510(k) Cleared Devices
Recent clearances: CURIS II RF Generator (REF 360100-05), FlexTip Bipolar electrodes single-use (AR-S9805-0028), FlexTip Bipolar electrodes single-use (AR-S9805-0035), Sutter Swyng non-stick bipolar forceps, single-use
9
Total
9
Cleared
0
Denied
FDA 510(k) Regulatory Record - Sutter Medizintechnik GmbH General & Plastic Surgery ✕
8 devices
Cleared
Feb 11, 2026
CURIS II RF Generator (REF 360100-05)
General & Plastic Surgery
243d
Cleared
Jan 25, 2024
FlexTip Bipolar electrodes single-use (AR-S9805-0028), FlexTip Bipolar...
General & Plastic Surgery
106d
Cleared
Feb 10, 2020
Sutter Swyng non-stick bipolar forceps, single-use
General & Plastic Surgery
49d
Cleared
Oct 04, 2019
Sutter Arrowtip Monopolar Electrodes
General & Plastic Surgery
58d
Cleared
Feb 23, 2018
Sutter CURIS RF Generator
General & Plastic Surgery
246d
Cleared
Sep 10, 2015
Sutter Bipolar Forceps-Calvian
General & Plastic Surgery
153d
Cleared
Aug 23, 2013
SUTTER BIPOLAR FORCEPS - SUPERGLISS
General & Plastic Surgery
134d
Cleared
Mar 17, 2008
SUTTER ELECTROSURGICAL CABLES
General & Plastic Surgery
98d