AKS Industries Inc.

FDA Device Registration & Listing · Scottsdale, AZ, US · Registration 3005665990

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
3005665990
FEI Number
3005665990
Entity Name
AKS Industries Inc.
City/State/Country
Scottsdale, AZ, US
Establishment Address
6991 E. Camelback Road, Suite D-216, Scottsdale, AZ 85251, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
AKS INDUSTRIES (Owner Number: 9083979)
Owner / Operator Contact Address
6991 East Camelback Road, Suite D-216, Scottsdale, AZ 85251, US
Initial Importer Flag
N
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
FNJ Bed, Manual General Hospital Class 1 880.5120 2020-11-06

Official Correspondent

Cindy Burns

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

AKS INDUSTRIES
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005665990. Last updated year: 2026. Please use registration number 3005665990 when referencing this establishment in official correspondence.
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