AVENDA HEALTH INC.

FDA Device Registration & Listing · Culver City, CA, US · Registration 3022983474

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
3022983474
FEI Number
3022983474
Entity Name
AVENDA HEALTH INC.
City/State/Country
Culver City, CA, US
Establishment Address
4130 Overland Ave, Culver City, CA 90230, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Avenda Health Inc. (Owner Number: 10086689)
Owner / Operator Contact Address
4130 Overland Ave, Culver City, CA 90230, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K221624
PMA Number
N/A

All Registered Proprietary Names

Unfold AI

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
POK Computer-Assisted Diagnostic Software For Lesions Suspicious For Cancer Radiology Class 2 892.2060 2022-12-02

Official Correspondent

Brittany Berry-Pusey

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Avenda Health Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K251769 Precision Medical Ventures, Inc. Dba Revealdx RevealAI-Lung 2026-01-30

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3022983474. Last updated year: 2026. Please use registration number 3022983474 when referencing this establishment in official correspondence.
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