Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017298490

FEI Number

3017298490

Entity Name

AUGUST BIOSERVICES, LLC

City/State/Country

Nashville, TN, US

Establishment Address

1845 Elm Hill Pike, Nashville, TN 37210, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

August Bioservices, LLC (Owner Number: 10091370)

Owner / Operator Contact Address

1845 Elm Hill Pike, Nashville, TN 37210, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KDN	System, Perfusion, Kidney	Gastroenterology, Urology	Class 2	876.5880	2024-09-09
KDL	Set, Perfusion, Kidney, Disposable	Gastroenterology, Urology	Class 2	876.5880	2024-09-09

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

August Bioservices, LLC

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 3017298490. Last updated year: 2026. Please use registration number 3017298490 when referencing this establishment in official correspondence.