Skip to the page
Get started free

Data / Medical devices / China / Weihai Dishang Medical Technology Co.,ltd

Weihai Dishang Medical Technology Co.,ltd: FDA-registered device maker in Weihai Shandong, China, 2 510(k) clearances

Weihai Dishang Medical Technology Co.,ltd is registered with the FDA (registration 3016680721) in Weihai Shandong, China. It lists 16 device types. The FDA files 2 510(k) clearances under its listings, the newest dated December 16, 2021. 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.

Get makers like this oneWatch Weihai Dishang Medical Technology Co.,ltd
FDA registration number
3016680721
Address
No.220-3 Huoju Road, Torch Hi-tech Industrial Development Zone, Weihai Shandong, China, 264200
Owner or operator
Weihai Dishang Medical Technology Co.,Ltd (10062870)
Roles
Contract manufacturer, Exporter to the US, Manufacturer
First device listed
March 12, 2020
Registered through
2026
Brand names listed
BRACE,THUMB,W/ADJ STRPS,RETAIL,UNIV,4/CS, CPE Gown, Copper infused filtered mask, DSAL1-WHITE, DSAL2-WHITE, Disposable Foam Knee/Body Strap, 4" x 60", Disposable Isolation Gown, Disposable Medical Operating Mask and more

Devices it lists

DeviceProduct codeClassRoleSource
Accessory, Surgical ApparelLYU1Exporter to the US, Manufactureraccessdata.fda.gov
Band Or Belt, Pelvic SupportISR1Exporter to the US, Manufactureraccessdata.fda.gov
Dress, SurgicalFYE1Exporter to the US, Manufactureraccessdata.fda.gov
Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella EuaQKRNExporter to the US, Manufactureraccessdata.fda.gov
Field Generator Positioning DeviceQLV1Exporter to the US, Manufactureraccessdata.fda.gov
Gown, ExaminationFME1Exporter to the US, Manufactureraccessdata.fda.gov
Gown, SurgicalFYA2Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Joint, Knee, External BraceITQ1Exporter to the US, Manufactureraccessdata.fda.gov
Mask, SurgicalFXX2Exporter to the US, Manufactureraccessdata.fda.gov
Non-Surgical GownOEA1Exporter to the US, Manufactureraccessdata.fda.gov
Orthosis, Limb BraceIQI1Exporter to the US, Manufactureraccessdata.fda.gov
Orthosis, LumbarIQE1Exporter to the US, Manufactureraccessdata.fda.gov
Protector, Skin PressureFMP1Exporter to the US, Manufactureraccessdata.fda.gov
Respirator, SurgicalMSH2Exporter to the US, Manufactureraccessdata.fda.gov
Support, ArmIOY1Exporter to the US, Manufactureraccessdata.fda.gov
Support, Patient PositionCCX1Exporter to the US, 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 16, 2021K210355Surgical Gown, Model: surgical gown-hp-3FYASubstantially EquivalentWeihai Dishang Medical Technology Co., Ltd.accessdata.fda.gov
October 24, 2021K210348Disposable Medical Surgical MaskFXXSubstantially EquivalentWeihai Dishang Medical Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated December 16, 2021. 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.