BLUR PRODUCT DEVELOPMENT

FDA Device Registration & Listing · Cary, NC, US · Registration 3014644251

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
3014644251
FEI Number
3014644251
Entity Name
BLUR PRODUCT DEVELOPMENT
City/State/Country
Cary, NC, US
Establishment Address
260 James Jackson Ave., Cary, NC 27513, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Blur Development Group (Owner Number: 10087809)
Owner / Operator Contact Address
260 James Jackson Ave., Cary, NC 27513, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

HPX Hyperpolarization System SurgiSight Amplio

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QVW Generator, Measurement, And/Or Delivery System For Hyperpolarized Mr Imaging Agents And Accessories, Cder Or Cber-Led Unknown Class N N/A 2023-04-12
FSO Microscope, Surgical, General & Plastic Surgery General, Plastic Surgery Class 1 878.4700 2023-10-30

Official Correspondent

Anthony Guazzo

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Blur Development Group
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 3014644251. Last updated year: 2026. Please use registration number 3014644251 when referencing this establishment in official correspondence.
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