Sutter Medizintechnik GmbH
Sutter Medizintechnik GmbH holds FDA 510(k) medical device clearances, first cleared 2008, most recent 2026, with 1 FDA device recall on record.
Top product codes for Sutter Medizintechnik GmbH
FDA recalls by Sutter Medizintechnik GmbH
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Sutter Medizintechnik GmbH
- K251813 — CURIS II RF Generator (REF 360100-05)
- K233425 — FlexTip Bipolar electrodes single-use (AR-S9805-0028), FlexTip Bipolar electrodes single-use (AR-S9805-0035)
- K193587 — Sutter Swyng non-stick bipolar forceps, single-use
- K192128 — Sutter Arrowtip Monopolar Electrodes
- K191732 — Sutter RaVoR Bipolar Electrodes
- K171869 — Sutter CURIS RF Generator
- K150959 — Sutter Bipolar Forceps-Calvian
- K131012 — SUTTER BIPOLAR FORCEPS - SUPERGLISS
- K073450 — SUTTER ELECTROSURGICAL CABLES
Data sourced from openFDA. This site is unofficial and independent of the FDA.