AURORA MANUFACTURING, LLC.

FDA Device Registration & Listing · Indianapolis, IN, US · Registration 3005529226

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
3005529226
FEI Number
3005529226
Entity Name
AURORA MANUFACTURING, LLC.
City/State/Country
Indianapolis, IN, US
Establishment Address
6330 East 75th Street, Suite 300, Indianapolis, IN 46250, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
AURORA MANUFACTURING, LLC. (Owner Number: 9080219)
Owner / Operator Contact Address
6330 East 75th Street, Suite 300, Indianapolis, IN 46250, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

HYDRO-AIRE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
INX Bed, Air Fluidized Physical Medicine Class 2 890.5160 2005-12-06

Official Correspondent

David Cole

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

AURORA MANUFACTURING, LLC.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005529226. Last updated year: 2026. Please use registration number 3005529226 when referencing this establishment in official correspondence.
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