Data / Medical devices / United States / NOAH MEDICAL Corp.

NOAH MEDICAL Corp.: FDA-registered device maker in Sunnyvale, CA, United States, 1 510(k) clearance

NOAH MEDICAL Corp. is registered with the FDA (registration 3027205723) in Sunnyvale, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 1, 2023. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number

3027205723

Address

1391 Geneva Dr, Sunnyvale, CA, United States, 94089

Owner or operator

Noah Medical (10087546)

Roles

Complaint file establishment, Specification developer

First device listed

March 13, 2023

Registered through

2026

Brand names listed

Galaxy System, Galaxy system bronchoscope and accessory kit

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.

Compare with other makers

• All makers of Bronchoscope (Flexible Or Rigid)

Updated March 1, 2023. 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.