Data / Medical devices / Switzerland / Corsano Health SA

Corsano Health SA: FDA-registered device maker in Plan-les-Ouates Geneve, Switzerland, 1 510(k) clearance

Name: Corsano Health SA FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Corsano Health SA is registered with the FDA (registration 3038761440) in Plan-les-Ouates Geneve, Switzerland. It lists 8 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 22, 2024. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3038761440
Address: Chemin de Pre' Fleuri 5, Plan-les-Ouates Geneve, Switzerland, 1228
Owner or operator: Corsano Health B.V. (10090535)
Roles: Manufacturer
First device listed: April 10, 2024
Registered through: 2026
Brand names listed: CardioWatch 287-2 System, Charge Station 10 Sensors A, Strap Silicon blue

Devices it lists

Device	Product code	Class	Role	Source
Continuous Measurement Thermometer	FLL	2	Manufacturer	accessdata.fda.gov
Monitor, Breathing Frequency	BZQ	2	Manufacturer	accessdata.fda.gov
Oximeter	DQA	2	Manufacturer	accessdata.fda.gov
Scale, Stand-On, Patient	FRI	1	Manufacturer	accessdata.fda.gov
Spirometer, Diagnostic	BZG	2	Manufacturer	accessdata.fda.gov
System, Measurement, Blood-Pressure, Non-Invasive	DXN	2	Manufacturer	accessdata.fda.gov
System, Network And Communication, Physiological Monitors	MSX	2	Manufacturer	accessdata.fda.gov
Transmitters And Receivers, Physiological Signal, Radiofrequency	DRG	2	Manufacturer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
March 22, 2024	K232548	Corsano CardioWatch 287-2 System	MSX	Substantially Equivalent	Corsano Health B.V.	accessdata.fda.gov

Compare with other makers

Updated March 22, 2024. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.