ANKON TECHNOLOGIES CO., LTD.

FDA Device Registration & Listing · Wuhan Hubei, CN · Registration 3017400296

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
3017400296
FEI Number
3017400296
Entity Name
ANKON TECHNOLOGIES CO., LTD.
City/State/Country
Wuhan Hubei, CN
Establishment Address
No. 666, Hi-tech Road, East Lake New Technology Development Zone, Wuhan Hubei 430073, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Ankon Technologies Co., Ltd. (Owner Number: 10077962)
Owner / Operator Contact Address
6010 W Spring Creek Parkway, Plano, TX 75024, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

NaviCam Xpress Stomach Capsule Endoscope System(NaviCam Xpress Stomach System)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QKZ Magnetically Maneuvered Capsule Endoscopy System Gastroenterology, Urology Class 2 876.1310 2021-10-28

Official Correspondent

No official correspondent registered.

US Agent Details

Tim Thomas Email: tim.thomas@anxrobotics.com Phone: (770) 4802911

Related Public Records

Same Entity

Ankon Technologies Co., Ltd.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Similar Registrations

Registration Number Establishment Name Location
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3015198783 ANKON MEDICAL TECHNOLOGIES (SHANGHAI) CO., LTD. Shanghai, CN
3028606342 OMAY(GUANGZHOU) MED TECHNOLOGIES CO., LTD Guangzhou Guangdong, CN
3038274470 BRAINMATTERZ, INC McKinney, TX, US
3012404174 LABORATORIO CHIMICO FARMACEUTICO A. SELLA SRL. Schio Vicenza, IT
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017400296. Last updated year: 2026. Please use registration number 3017400296 when referencing this establishment in official correspondence.
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