Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3021604067

FEI Number

3021604067

Entity Name

NINGBO VERYKIND MEDICAL DEVICE CO., LTD.

City/State/Country

Ningbo Zhejiang, CN

Establishment Address

#100 Jinghua Road, High-tech, Industrial Development Zone Ningbo, 315040 Zhejiang, P.R. China, Ningbo Zhejiang 315040, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Ningbo Verykind Medical Device Co., Ltd. (Owner Number: 10083880)

Owner / Operator Contact Address

#100 Jinghua Road, High-tech, Industrial Development Zone Ningbo, 315040 Zhejiang, P.R. China, Ningbo, CN-ZJ 315040, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K211458

PMA Number

N/A

All Registered Proprietary Names

David Staplers

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GDW	Staple, Implantable	General, Plastic Surgery	Class 2	878.4750	2022-01-04
GAG	Stapler, Surgical	General Hospital	Class 2	878.4740	2022-01-04

Official Correspondent

MI ZHAO

US Agent Details

WINNIE Zhu Business: Umedwings Solution USA Email: Agent@Umedwings.Us Phone: (224) 4023150

Related Public Records

Same Entity

Ningbo Verykind Medical Device Co., 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
K131563	Opus Ksd, Inc.	SUBQ IT! BIOABSORBABLE SKIN CLOSURE SYSTEM	2014-04-09
K131705	Covidien, Formerly US Surgical A Divison of Tyco H	ENDO GIA RADIAL RELOAD WITH TRI-STAPLE TECHNOLOGY	2013-07-01
K103263	Covidien, Formerly US Surgical A Divison of Tyco H	ENDO GIA SINGLEUSE DUET TRS RELOAD WITH TRI0STAPLE TECHNOLOGY	2010-11-22
K130717	Covidien, Formerly US Surgical A Divison of Tyco H	ENDO GIA RELOAD	2013-04-18
K221006	Covidien	GIA Stapler with Tri-Staple Technology	2022-04-29

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0001-2021	N/A	2	Endo GIA Auto Suture Gray Universal Articulating Loading Unit 30 mm - 2.0 mm, Item Code 030450 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection and creation of anastomosis.
Z-0002-2021	N/A	2	Endo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 2.5 mm, Item Code 030451 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection and creation of anastomosis.
Z-0003-2021	N/A	2	Endo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 3.5 mm, Item Code 030452 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection and creation of anastomosis.
Z-0004-2021	N/A	2	Endo GIA Auto Suture Universal Articulating Loading Unit 45 mm - 2.0 mm, Item Code 030453 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection and creation of anastomosis.
Z-0005-2021	N/A	2	Endo GIA Auto Suture Universal Loading Unit 45 mm - 2.5mm, Item Code 030454 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection and creation of anastomosis.

Similar Registrations

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3013942591	INTUITIVE SURGICAL, INC.	Sunnyvale, CA, US
1219930	Covidien	North Haven, CT, US
3015612252	INTUITIVE SURGICAL, INC.	Santa Clara, CA, US
3013283620	Intuitive Surgical G.K.	Tokyo, JP

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3021604067. Last updated year: 2026. Please use registration number 3021604067 when referencing this establishment in official correspondence.