Kelvi

FDA Device Registration & Listing · Inglewood, CA, US · Registration 3015252349

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
3015252349
FEI Number
3015252349
Entity Name
Kelvi
City/State/Country
Inglewood, CA, US
Establishment Address
413 N Oak Street, Inglewood, CA 90302, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Hypothermia Devices, Inc. (dba Kelvi) (Owner Number: 10058108)
Owner / Operator Contact Address
413 N Oak Street, Inglewood, CA 90302, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Kelvi Pro-e Kelvi Pro

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ILO Pack, Hot Or Cold, Water Circulating Physical Medicine Class 2 890.5720 2018-07-10

Official Correspondent

Julio Vergara

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Hypothermia Devices, Inc. (dba Kelvi)
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 3015252349. Last updated year: 2026. Please use registration number 3015252349 when referencing this establishment in official correspondence.
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