Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010594949

FEI Number

3010594949

Entity Name

Hunan Handlike Minimally Invasive Surgery Co., Ltd.

City/State/Country

Changsha Hunan, CN

Establishment Address

A4,Lugu Yuyuan,#27,Wenxuan Rd,High-tech Zone, Changsha Hunan 410205, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Hunan Handlike Minimally Invasive Surgery Co.,Ltd. (Owner Number: 10045334)

Owner / Operator Contact Address

A4,Lugu Yuyuan,#27,Wenxuan Rd,High-tech Zone, Changsha, CN-HN 410205, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Ultrasonic Surgical System, model HD-CSXT-001 Laparoscopic accessories Curved Needle Holder (Single Action), Reference code HD1020431, HD1020401 Cholangiography Forceps, Reference code HD1010116, HD1020116, HD1010106, HD1010136 Straight Needle Holder (Single Action), Reference code HD1020432, HD1020402

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LFL	Instrument, Ultrasonic Surgical	Unknown	Class U	N/A	2024-06-20
NWV	Laparoscopic Accessories, Gynecologic	Obstetrics/Gynecology	Class 1	884.1720	2013-11-06

Official Correspondent

Jiajie Yan

US Agent Details

Simin Lin Email: simin_lin123@126.com Phone: (415) 6026843

Related Public Records

Same Entity

Hunan Handlike Minimally Invasive Surgery Co.,Ltd.

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-0332-2022	Covidien Llc	U	Covidien Sonicision Battery Charger-intended to charge the Sonicision Reusable Battery Pack and to provide information on the battery charging progress and battery pack status Item Code: CBCA

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010594949. Last updated year: 2026. Please use registration number 3010594949 when referencing this establishment in official correspondence.