Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3020969413

FEI Number

3020969413

Entity Name

Nevro Medical S.R.L.

City/State/Country

El Coyol Alajuela, CR

Establishment Address

Building 28-C, Coyol Free Zone Park C.R, El Coyol Alajuela 20101, CR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Globus Medical, Inc (Owner Number: 10030390)

Owner / Operator Contact Address

2560 GENERAL ARMISTEAD AVE., VALLEY FORGE BUSINESS CENTER, Audubon, PA 19403, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

P130022

All Registered Proprietary Names

Senza Spinal Cord Stimulation (SCS) System

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
QRB	Stimulator, Spinal-Cord, Totally Implanted For Relief Of Pain Due To Diabetic Neuropathy	Unknown	Class 3	N/A	2015-05-12
LGW	Stimulator, Spinal-Cord, Totally Implanted For Pain Relief	Unknown	Class 3	N/A	2015-05-12

Official Correspondent

Daniel S Paul

US Agent Details

Daniel S Paul Email: dspaul@globusmedical.com Phone: (610) 9301800

Related Public Records

Same Entity

Globus Medical, Inc

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3008514029	NEVRO CORP.	Redwood City, CA, US

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0022-2018	St. Jude Medical, Inc.	3	Proclaim 5 Elite Implantable Pulse Generator and Proclaim 7 Elite Implantable Pulse Generator Models 3660, 3661, 3662, 3663, 3665, 3667
Z-0024-2018	St. Jude Medical, Inc.	3	Proclaim DRG Implantable Pulse Generator Model 3664
Z-0025-2013	Advanced Neuromodulation Systems Inc.	3	The Eon Mini Implantable Pulse Generator (IPG) is a 16-channel, rechargeable, multi-program system that allows the connection of one or two leads with four, eight, and 16 electrode leads. It is powered by a hermetically sealed battery within a titanium case. It uses microelectronic circuitry to generate constant current electrical stimulation. Stimulation programs can be delivered as either single stimulation or MultiStim programs depending on patients need. Product Usage: Eon Mini system is indicated as an aid in the management of chronic intractable pain of the trunk and/or limbs including unilateral or bilateral pain associated with the following: failed back surgery syndrome, intractable low back and leg pain.
Z-0458-2026	Abbott Medical	3	Eterna SCS IPG (Implantable Pulse Generator), Model Number 32400
Z-2358-2024	Abbott Medical	3	Abbott Proclaim XR 5 Implantable Pulse Generator, REF 3660, Sterile EO, Rx Only

Similar Registrations

Registration Number	Establishment Name	Location
3008514029	NEVRO CORP.	Redwood City, CA, US
3015173212	Medline Industries, LP - Mexicali (MXC)	Mexicali Baja California, MX
2182207	MEDTRONIC NEUROMODULATION	Minneapolis, MN, US
3021836309	Saluda Medical Pty. Ltd.	Macquarie Park New South Wales, AU
2133641	BENCHMARK ELECTRONICS, INC.	WINONA, MN, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3020969413. Last updated year: 2026. Please use registration number 3020969413 when referencing this establishment in official correspondence.