Skip to the page

Data / Medical devices / China / Ningbo Haishu Zonghai Artware Co., Ltd.

Ningbo Haishu Zonghai Artware Co., Ltd.: FDA-registered device maker in Ningbo City Zhejiang, China, 1 510(k) clearance

Ningbo Haishu Zonghai Artware Co., Ltd. is registered with the FDA (registration 3009694272) in Ningbo City Zhejiang, China. It lists 6 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 9, 2016. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3009694272
Address
Guangsheng Village, Jishigang Town Haishu District, Ningbo City Zhejiang, China, 315172
Owner or operator
Ningbo Haishu Zonghai Artware Co., Ltd. (10041107)
Roles
Contract manufacturer, Manufacturer
First device listed
June 20, 2012
Registered through
2026
Brand names listed
AM/PM Weekly Pill Box, Brace Gard Mini Pak / 79/6DP, Brace Relief Pocket Kit,/ 79/2DP, Brace Relief Pocket Kit,/ 79/DP, Brace Relief Quads, CHROME ULTRA GRIP BATH HANDLE 12" INDICATOR FOR SECURITY, Contact Lens Case, ECONOMY AM/PM WEEKLY PILL BOX and more

Devices it lists

DeviceProduct codeClassRoleSource
Adaptor, HygieneILS1Contract manufacturer, Manufactureraccessdata.fda.gov
Aid, TransferIKX1Contract manufacturer, Manufactureraccessdata.fda.gov
Case, Contact LensLRX2Manufactureraccessdata.fda.gov
Dispenser, Solid MedicationNXB1Contract manufacturer, Manufactureraccessdata.fda.gov
Pill Crusher/CutterOHY1Contract manufacturer, Manufactureraccessdata.fda.gov
Wax, Dental, IntraoralEGD1Contract manufacturer, Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
December 9, 2016K162869Contact Lens CaseLRXSubstantially EquivalentNingbo Yinzhou Zonghai Artware Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated December 9, 2016. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.