Ningbo Skonsin Electronics Ltd.

FDA Device Registration & Listing · Ningbo Zhejiang, CN · Registration 3035781529

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
3035781529
FEI Number
3035781529
Entity Name
Ningbo Skonsin Electronics Ltd.
City/State/Country
Ningbo Zhejiang, CN
Establishment Address
Bldg 1,No. 655 Wenshui Rd, Yinzhou Dist, Ningbo, Zhejiang, China, Ningbo Zhejiang 315100, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Ningbo Skonsion Electronics Ltd. (Owner Number: 10092337)
Owner / Operator Contact Address
Building 1,No. 655 Wenshui Road, Yinzhou District, Ningbo, Zhejiang Province, China, 2F & 3F, Building 1, No. 99, Mingguang Road, Shounan Street, Yinzhou District, Ningbo City, Zhejiang Province, Ningbo, CN-ZJ 315100, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

ClearVision Single Use Hysteroscope & Image Processing System (EHS-Dx4001, EHS-Op5001, EHS-Op6001, EHS-IPS01US)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HIH Hysteroscope (And Accessories) Obstetrics/Gynecology Class 2 884.1690 2024-12-25

Official Correspondent

Xinxia Tong

US Agent Details

hui hong Business: ABMED MEDICAL TECHNOLOGY INC Email: info@abmed.us Phone: (509) 5816099

Related Public Records

Same Entity

Ningbo Skonsion Electronics Ltd.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K935716 KARL STORZ Endoscopy-America, Inc. KARL STORZ FIXED MAGNIFICATION TELESCOPE/KS VARIABLE MAGNIFICATION TELESCOPE 1995-11-16

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3035781529. Last updated year: 2026. Please use registration number 3035781529 when referencing this establishment in official correspondence.
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