SOULAIRE CORPORATION

FDA Device Registration & Listing · Los Angeles, CA, US · Registration 3017791225

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
3017791225
FEI Number
3017791225
Entity Name
SOULAIRE CORPORATION
City/State/Country
Los Angeles, CA, US
Establishment Address
7911 Beach Street, Unit 5, Los Angeles, CA 90001, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Soulaire Corporation (Owner Number: 10079606)
Owner / Operator Contact Address
1934 14TH Street, Unit A, Santa Monica, CA 90404, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K202108
PMA Number
N/A

All Registered Proprietary Names

Soulaire

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DRN Device, Counter-Pulsating, External Cardiovascular Class 2 870.5225 2024-12-12

Official Correspondent

Morad Soulati

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Soulaire Corporation
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 3017791225. Last updated year: 2026. Please use registration number 3017791225 when referencing this establishment in official correspondence.
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