ANACOM GENERAL CORPORATION

FDA Device Registration & Listing · Anaheim, CA, US · Registration 1000125358

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
1000125358
FEI Number
1000125358
Entity Name
ANACOM GENERAL CORPORATION
City/State/Country
Anaheim, CA, US
Establishment Address
1240 S. Claudina St., Anaheim, CA 92805, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
Anacom General Corporation (Owner Number: 10057262)
Owner / Operator Contact Address
1240 S. Claudina St., Anaheim, CA 92805, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Series 8 Series 7

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ILQ System, Communication, Powered Physical Medicine Class 2 890.3710 2018-03-13

Official Correspondent

Joe Kuciera

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Anacom General Corporation
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0004-2016 Lifeline Systems, Incorporated 2
Philips GoSafe Mobile Help Button; 7000MHB. Personal Emergency Response System.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000125358. Last updated year: 2026. Please use registration number 1000125358 when referencing this establishment in official correspondence.
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