MAGNET MEDICAL SYSTEMS LLC

FDA Device Registration & Listing · Southlake, TX, US · Registration 3028240331

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
3028240331
FEI Number
3028240331
Entity Name
MAGNET MEDICAL SYSTEMS LLC
City/State/Country
Southlake, TX, US
Establishment Address
300 State St., 93281, Southlake, TX 76092, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Magnet Medical Systems LLC (Owner Number: 10088883)
Owner / Operator Contact Address
1910 Thomes Ave, 93281, Cheyenne, WY 82001, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

ProBio Select ProBio Collect ProBio Collect

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LXG Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use Clinical Chemistry Class 1 862.2050 2024-04-02
KYX Dispenser, Liquid Medication General Hospital Class 1 880.6430 2024-04-02
LGX Table, Examination, Medical, Powered General, Plastic Surgery Class 1 878.4960 2024-04-02

Official Correspondent

Sanjay Malkani

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Magnet Medical Systems LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0002-2008 Beckman Coulter Inc 1
FP1000 Cell Preparation System Software versions 1.1 & 1.2, Part Number 624922, for in vitro diagnostic use.
Z-0023-2013 Biomerieux Inc 1
PREVI Isola System, Catalog numbers 29500 and 29500R, bioMerieux, Inc., Durham, NC. Intended to perform the inoculation and streaking of Prepoured Media (PPM) with liquid microbiological samples.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3028240331. Last updated year: 2026. Please use registration number 3028240331 when referencing this establishment in official correspondence.
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