LIFECYCLE BIOTECHNOLOGIES, LLC

FDA Device Registration & Listing · Cleburne, TX, US · Registration 3020224798

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
3020224798
FEI Number
3010877980
Entity Name
LIFECYCLE BIOTECHNOLOGIES, LLC
City/State/Country
Cleburne, TX, US
Establishment Address
421 Marti Drive, Cleburne, TX 76033, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Lifecycle Biotechnologies, LP (Owner Number: 10049711)
Owner / Operator Contact Address
421 Marti Drive, Cleburne, TX 76033, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Belzer UW® Cold Storage Solution Purified Water, Isopropyl Alcohol 70%, Hydrochloric Acid Blends, Phosphate Buffer Blends, Sodium Chloride Blends Belzer MPS (UW Machine Perfusion Solution) EasiSlush

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KDL Set, Perfusion, Kidney, Disposable Gastroenterology, Urology Class 2 876.5880 2025-11-21
KDN System, Perfusion, Kidney Gastroenterology, Urology Class 2 876.5880 2025-11-21
PPM General Purpose Reagent Pathology Class 1 864.4010 2015-07-15
KDN System, Perfusion, Kidney Gastroenterology, Urology Class 2 876.5880 2026-04-15
KDN System, Perfusion, Kidney Gastroenterology, Urology Class 2 876.5880 2025-08-18

Official Correspondent

Michelle Stahla-Quintana

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Lifecycle Biotechnologies, LP
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
K013575 Organ Recovery Systems, Inc. KPS-I, THE KIDNEY PERFUSION SOLUTION 2002-01-25

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3020224798. Last updated year: 2026. Please use registration number 3020224798 when referencing this establishment in official correspondence.
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