Veranex, Inc.

FDA Device Registration & Listing · Providence, RI, US · Registration 300643947

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
300643947
FEI Number
3006463947
Entity Name
Veranex, Inc.
City/State/Country
Providence, RI, US
Establishment Address
55 DUPONT DR, Providence, RI 02907, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
Veranex, Inc. (Owner Number: 10023193)
Owner / Operator Contact Address
55 Dupont Drive, Providence, RI 02907, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Arctic Frost

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KYR Bag, Ice General Hospital Class 1 880.6050 2025-07-31

Official Correspondent

Corie Vazquez

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Veranex, Inc.
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 300643947. Last updated year: 2026. Please use registration number 300643947 when referencing this establishment in official correspondence.
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