Data / Medical devices / Canada / Siaron Medical Ltd

Siaron Medical Ltd: FDA-registered device maker in Vancouver British Columbia, Canada, 2 510(k) clearances

Name: Siaron Medical Ltd FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Siaron Medical Ltd is registered with the FDA (registration 3012169560) in Vancouver British Columbia, Canada. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated November 6, 2018. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get makers like this one Watch Siaron Medical Ltd

FDA registration number: 3012169560
Address: 8392 Prince Edward St, Vancouver British Columbia, Canada, V5X 3R9
Owner or operator: Siaron Medical Ltd (10052905)
Roles: Exporter to the US
First device listed: December 1, 2017
Registered through: 2026
Brand names listed: Siemens Healthcare

Devices it lists

Device	Product code	Class	Role	Source
Coil, Magnetic Resonance, Specialty	MOS	2	Exporter to the US	accessdata.fda.gov
System, Nuclear Magnetic Resonance Imaging	LNH	2	Exporter to the US	accessdata.fda.gov
System, Nuclear Magnetic Resonance Spectroscopic	LNI	2	Exporter to the US	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
November 6, 2018	K181613	MAGNETOM Avanto, MAGNETOM Verio with software syngo MR E11D	LNH	Substantially Equivalent	Siemens Medical Solutions USA, Inc.	accessdata.fda.gov
October 16, 2003	K032428	MAGNETOM AVANTO MR SYSTEM	LNH	Substantially Equivalent	Siemens Medical Solutions USA, Inc.	accessdata.fda.gov

Compare with other makers

Updated November 6, 2018. 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.