Skip to the page
Get started free

Data / Medical devices / China / Guangxi Ehall Medical Technology Co.,ltd

Guangxi Ehall Medical Technology Co.,ltd: FDA-registered device maker in Nanning Guangxi, China, 1 510(k) clearance

Guangxi Ehall Medical Technology Co.,ltd is registered with the FDA (registration 3036269993) in Nanning Guangxi, China. It lists 17 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 11, 2025. Registered through 2026. FDA data exported November 3, 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 Guangxi Ehall Medical Technology Co.,ltd
FDA registration number
3036269993
Address
6F, Kechuan Blgd, 25-1, Keyuan Road, Nanning Guangxi, China, 530012
Owner or operator
Guangxi Ehall Medical Technology Co.,Ltd (10092754)
Roles
Exporter to the US, Manufacturer
First device listed
February 14, 2025
Registered through
2026
Brand names listed
Absorbent Paper Points, Gutta Percha Points, Capillary Tip, 3 Way Air Syringe, Air Water Syringe, Saliva Ejector, Cheek Retractor, Silicone Cheek Retractor, Composite Heater, Cotton Roll, Cotton Gauze, Dental Dib, Face Protetive Paper, Dental Box, Denture Box, Cotton Roll Dispenser, Dental Implant Torque Wrench, Dental Implant Unit and more

Devices it lists

DeviceProduct codeClassRoleSource
Accessories, Implant, Dental, EndosseousNDP1Exporter to the US, Manufactureraccessdata.fda.gov
Applicator, ResinKXR1Exporter to the US, Manufactureraccessdata.fda.gov
Cleaner, Ultrasonic, Medical InstrumentFLG1Exporter to the US, Manufactureraccessdata.fda.gov
Controller, Foot, Handpiece And CordEBW1Exporter to the US, Manufactureraccessdata.fda.gov
Cotton, RollEFN1Exporter to the US, Manufactureraccessdata.fda.gov
Device, Heat-SealingKSD1Exporter to the US, Manufactureraccessdata.fda.gov
Heat Source For Bleaching TeethEEG1Exporter to the US, Manufactureraccessdata.fda.gov
Instrument, Manual, Surgical, General UseMDM1Exporter to the US, Manufactureraccessdata.fda.gov
Instruments, Dental HandDZN1Exporter to the US, Manufactureraccessdata.fda.gov
Loupe, Diagnostic/SurgicalFSP1Exporter to the US, Manufactureraccessdata.fda.gov
Point, Paper, EndodonticEKN1Exporter to the US, Manufactureraccessdata.fda.gov
Retractor, All TypesEIG1Exporter to the US, Manufactureraccessdata.fda.gov
Strip, Polishing AgentEHM1Exporter to the US, Manufactureraccessdata.fda.gov
Syringe, Irrigating (Dental)EIB1Exporter to the US, Manufactureraccessdata.fda.gov
Syringe, Periodontic, Endodontic, IrrigatingEIC1Exporter to the US, Manufactureraccessdata.fda.gov
Unit, Operative Dental, AccessoriesNRD1Exporter to the US, Manufactureraccessdata.fda.gov
Wire, OrthodonticDZC1Exporter 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
April 11, 2025K242646Dental Implant UnitEBWSubstantially EquivalentGuilin Aesthedent Medical Instruments Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated April 11, 2025. 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.