BLUEPRINT MANUFACTURING CORPORATION

FDA Device Registration & Listing · Irvine, CA, US · Registration 3042902796

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
3042902796
FEI Number
3042902796
Entity Name
BLUEPRINT MANUFACTURING CORPORATION
City/State/Country
Irvine, CA, US
Establishment Address
9272 Jeronimo Rd Ste 111, Irvine, CA 92618, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Blueprint Manufacturing Corporation (Owner Number: 10094589)
Owner / Operator Contact Address
9272 Jeronimo Rd, Suite 111, Irvine, CA 92618, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

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 2025-12-09

Official Correspondent

Nicholas Hu

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Blueprint Manufacturing Corporation
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 3042902796. Last updated year: 2026. Please use registration number 3042902796 when referencing this establishment in official correspondence.
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