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Data / Medical devices / United States / Nevro Corp.

Nevro Corp.: FDA-registered device maker in Redwood City, CA, United States, 1 PMA approval

Nevro Corp. is registered with the FDA (registration 3008514029) in Redwood City, CA, United States. It lists 2 device types. The FDA files 1 PMA approval under its listings, the newest dated May 8, 2015. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number
3008514029
Address
1800 Bridge Pkwy, Redwood City, CA, United States, 94065
Owner or operator
Globus Medical, Inc (10030390)
Roles
Manufacturer
First device listed
May 12, 2015
Registered through
2027
Brand names listed
Senza Spinal Cord Stimulation (SCS) System

Devices it lists

PMA approvals

Premarket approvals this establishment lists, with the supplements the FDA has decided since.

ApprovedPMA numberDeviceProduct codeSupplementsLatest decisionSource
May 8, 2015P130022NEVRO SENZA SPINAL CORD STIMULATION (SCS) SYSTEMLGW63August 18, 2026accessdata.fda.gov

Compare with other makers

Updated August 18, 2026. 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.