HEARTLUNG CORPORATION

FDA Device Registration & Listing · Houston, TX, US · Registration 3039211310

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
3039211310
FEI Number
3039211310
Entity Name
HEARTLUNG CORPORATION
City/State/Country
Houston, TX, US
Establishment Address
2450 Holcombe Blvd, Houston, TX 77021, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
HeartLung Corporation (Owner Number: 10093760)
Owner / Operator Contact Address
2450 Holcombe Blvd, Houston, TX 77021, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K213760
PMA Number
N/A

All Registered Proprietary Names

AutoBMD

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KGI Densitometer, Bone Radiology Class 2 892.1170 2025-07-03

Official Correspondent

Morteza Naghavi

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

HeartLung Corporation
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
K983273 Medical Systems, Inc. XCT 2000 L PQCT BONE DENSITOMETER 1998-10-29

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3039211310. Last updated year: 2026. Please use registration number 3039211310 when referencing this establishment in official correspondence.
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