ATHFAR 828, Inc.

FDA Device Registration & Listing · Big Rapids, MI, US · Registration 3012047128

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
3012047128
FEI Number
3012047128
Entity Name
ATHFAR 828, Inc.
City/State/Country
Big Rapids, MI, US
Establishment Address
605 S. Third Avenue, Suite C, Big Rapids, MI 49307, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
ATHFAR 828, Inc. (Owner Number: 10050266)
Owner / Operator Contact Address
274 West Cortland Street, Jackson, MI 49201, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Silent Night, LLC AIRO

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FRL Fiber, Medical, Absorbent General Hospital Class 1 880.5300 2015-10-27

Official Correspondent

BOB RUTAN

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ATHFAR 828, Inc.
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 3012047128. Last updated year: 2026. Please use registration number 3012047128 when referencing this establishment in official correspondence.
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