BRANCHPOINT

FDA Device Registration & Listing · Placentia, CA, US · Registration 3023540124

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
3023540124
FEI Number
3023540124
Entity Name
BRANCHPOINT
City/State/Country
Placentia, CA, US
Establishment Address
570 S Melrose St, Placentia, CA 92870, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Branchpoint & Aura Development LLC (Owner Number: 10089340)
Owner / Operator Contact Address
570 S Melrose St, Placentia, CA 92870, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K172209
PMA Number
N/A

All Registered Proprietary Names

AURA

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GWM Device, Monitoring, Intracranial Pressure Neurology Class 2 882.1620 2023-11-29

Official Correspondent

Erin Hickey

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Branchpoint & Aura Development LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K020558 Integra Neurosciences LICOX CC1.G2 BRAIN OXYGEN CATHETER-MICROPROBE 2002-03-21

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3023540124. Last updated year: 2026. Please use registration number 3023540124 when referencing this establishment in official correspondence.
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