Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017987352

FEI Number

3017987352

Entity Name

Spark Biomedical Inc.

City/State/Country

Richmond, TX, US

Establishment Address

7535 W Grand Pkwy S, Richmond, TX 77407, US

Establishment Type(s)

Manufacture Medical Device,Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198

Owner / Operator

Spark Biomedical Inc (Owner Number: 10080441)

Owner / Operator Contact Address

18208 Preston Road, Ste D9-531, Dallas, TX 75252, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K251246

PMA Number

N/A

All Registered Proprietary Names

Sparrow Ascent

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PZR	Percutaneous Nerve Stimulator For Opioid Withdrawal	Neurology	Class 2	882.5896	2026-01-08

Official Correspondent

Brent Croft

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Spark Biomedical Inc

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017987352. Last updated year: 2026. Please use registration number 3017987352 when referencing this establishment in official correspondence.