ANP TECHNOLOGIES INC

FDA Device Registration & Listing · Newark, DE, US · Registration 3004181896

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
3004181896
FEI Number
3004181896
Entity Name
ANP TECHNOLOGIES INC
City/State/Country
Newark, DE, US
Establishment Address
824 Interchange Blvd, Newark, DE 19711, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
ANP Technologies Inc (Owner Number: 10085418)
Owner / Operator Contact Address
824 Interchange Blvd, Newark, DE 19711, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

NIDS COVID-19 Antigen Rapid Test Kit

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QKP Coronavirus Antigen Detection Test System. Unknown Class N N/A 2022-06-21

Official Correspondent

Greg Witham

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ANP Technologies Inc
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-0001-2023 Jiangsu Well Biotech Co., Ltd. No N
Jiangsu Well Biotech Co.,Ltd. AND SDI LABS COVID-19 Ag Rapid Test Device - Cat#: CO-02

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004181896. Last updated year: 2026. Please use registration number 3004181896 when referencing this establishment in official correspondence.
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