NEUROVENTION, LLC

FDA Device Registration & Listing · Daytona Beach, FL, US · Registration 3017884860

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
3017884860
FEI Number
3017884860
Entity Name
NEUROVENTION, LLC
City/State/Country
Daytona Beach, FL, US
Establishment Address
645 S. Beach St, Daytona Beach, FL 32114, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
NeuroVention, LLC (Owner Number: 10080022)
Owner / Operator Contact Address
645 S. Beach St, Daytona Beach, FL 32114, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K192162
PMA Number
N/A

All Registered Proprietary Names

DC Plate KTC Burr Hole Cover NuCrani Plates Rescue Screw Torx Slot Driver bit Torx Screw Torx Slot Drill bit Screwdriver Tray Driver bit Torx Slot

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GWO Plate, Cranioplasty, Preformed, Alterable Neurology Class 2 882.5320 2021-01-07
GXR Cover, Burr Hole Neurology Class 2 882.5250 2021-01-07
HBW Fastener, Plate, Cranioplasty Neurology Class 2 882.5360 2021-01-07

Official Correspondent

Rohit Khanna

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

NeuroVention, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017884860. Last updated year: 2026. Please use registration number 3017884860 when referencing this establishment in official correspondence.
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