VIRGO USA R&D CORP

FDA Device Registration & Listing · Great Neck, NY, US · Registration 3042751292

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
3042751292
FEI Number
3042751292
Entity Name
VIRGO USA R&D CORP
City/State/Country
Great Neck, NY, US
Establishment Address
39 South drive Great Neck NY 11021, Great Neck, NY 11021, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
VIRGO USA R&D CORP (Owner Number: 10094583)
Owner / Operator Contact Address
39 South drive Great Neck NY 11021, Great Neck, NY 11021, 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
PTY Computerized Cognitive Assessment Aid, Exempt Neurology Class 2 882.1470 2025-12-09

Official Correspondent

Yan Zhang

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

VIRGO USA R&D CORP
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 3042751292. Last updated year: 2026. Please use registration number 3042751292 when referencing this establishment in official correspondence.
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