NEUROVICE

FDA Device Registration & Listing · Charlotte, NC, US · Registration 3042640302

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3042640302
FEI Number
3042640302
Entity Name
NEUROVICE
City/State/Country
Charlotte, NC, US
Establishment Address
1235 East Blvd Ste E, Pmb 2001, Charlotte, NC 28203, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
NeuroVice (Owner Number: 10094705)
Owner / Operator Contact Address
1235 East Blvd Suite E, PMB 2001, Charlotte, NC 28203, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

PATI Protector Against Tongue Injury (PATI)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JXL Block, Bite Neurology Class 2 882.5070 2025-12-17

Official Correspondent

Jordan Schindler

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

NeuroVice
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 3042640302. Last updated year: 2026. Please use registration number 3042640302 when referencing this establishment in official correspondence.
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