ALPHA TEKNIKO

FDA Device Registration & Listing · Lake Zurich, IL, US · Registration 3007798904

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
3007798904
FEI Number
3007798904
Entity Name
ALPHA TEKNIKO
City/State/Country
Lake Zurich, IL, US
Establishment Address
1400 Rose RD, Lake Zurich, IL 60047, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Alpha Bedding LLC DBA Alpha Tekniko (Owner Number: 10030127)
Owner / Operator Contact Address
1290 Ensell Road, Lake Zurich, IL 60047, 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
FMW Cover, Mattress (Medical Purposes) General Hospital Class 1 880.6190 2010-12-30
IKY Mattress, Flotation Therapy, Non-Powered General Hospital Class 1 880.5150 2009-08-17
IMP Cushion, Wheelchair Physical Medicine Class 1 890.3920 2014-06-03
FNM Mattress, Air Flotation, Alternating Pressure General Hospital Class 2 880.5550 2015-02-16

Official Correspondent

Ted Lazakis

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Alpha Bedding LLC DBA Alpha Tekniko
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 3007798904. Last updated year: 2026. Please use registration number 3007798904 when referencing this establishment in official correspondence.
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