Data / Medical devices / Switzerland / Sensimed SA

Sensimed SA: FDA-registered device maker in Etagnieres Vaud, Switzerland, 1 510(k) clearance

Sensimed SA is registered with the FDA (registration 3008727434) in Etagnieres Vaud, Switzerland. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 4, 2016. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number

3008727434

Address

Route en Rambuz 17, Etagnieres Vaud, Switzerland, 1037

Owner or operator

Sensimed SA (10054686)

Roles

Manufacturer

First device listed

April 14, 2017

Registered through

2026

Brand names listed

Triggerfish

Devices it lists

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.

Updated March 4, 2016. 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.