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Data / Medical devices / China / Dentalmaster (xiamen) Medical Technology Co., Ltd.

Dentalmaster (xiamen) Medical Technology Co., Ltd.: FDA-registered device maker in Xiamen Fujian, China, 1 510(k) clearance

Dentalmaster (xiamen) Medical Technology Co., Ltd. is registered with the FDA (registration 3049848767) in Xiamen Fujian, China. It lists 25 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 24, 2026. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3049848767
Address
No.19-2, Dingshan Middle Road, Haicang District, Xiamen Fujian, China, 361027
Owner or operator
DentalMaster (Xiamen) Medical Technology Co., Ltd. (10096306)
Roles
Manufacturer
First device listed
August 31, 2026
Registered through
2026
Brand names listed
Angled bone clamp, Blade, Blade (plastic), Bone Bur, Bone Carrier, Bone Chisel, Bone Clamp, Bone Condenser and more

Devices it lists

DeviceProduct codeClassRoleSource
Accessories, Retractor, DentalEIF1Manufactureraccessdata.fda.gov
Carver, Dental Amalgam, OperativeEKH1Manufactureraccessdata.fda.gov
Chisel, Bone, SurgicalEML1Manufactureraccessdata.fda.gov
Curette, PeriodonticEMS1Manufactureraccessdata.fda.gov
Curette, Surgical, DentalEMK1Manufactureraccessdata.fda.gov
Drill, Dental, IntraoralDZA1Manufactureraccessdata.fda.gov
Driver, Band, OrthodonticECT1Manufactureraccessdata.fda.gov
Elevator, Surgical, DentalEMJ1Manufactureraccessdata.fda.gov
Explorer, OperativeEKB1Manufactureraccessdata.fda.gov
File, Pulp Canal, EndodonticEKS1Manufactureraccessdata.fda.gov
Forceps, Dressing, DentalEFL1Manufactureraccessdata.fda.gov
Forceps, Rongeur, SurgicalEMH1Manufactureraccessdata.fda.gov
Gauge, Depth, Instrument, DentalEIL1Manufactureraccessdata.fda.gov
Handle, Instrument, DentalEJB1Manufactureraccessdata.fda.gov
Hemostat, SurgicalEMD1Manufactureraccessdata.fda.gov
Instrument, Diamond, DentalDZP1Manufactureraccessdata.fda.gov
Mirror, MouthEAX1Manufactureraccessdata.fda.gov
ParallelometerEGI1Manufactureraccessdata.fda.gov
Plugger, Root Canal, EndodonticEKR1Manufactureraccessdata.fda.gov
Scissors, Surgical Tissue, DentalEGN1Manufactureraccessdata.fda.gov
Screw, Fixation, IntraosseousDZL2Manufactureraccessdata.fda.gov
Spreader, Pulp Canal Filling Material, EndodonticEKK1Manufactureraccessdata.fda.gov
Stylet For Catheter, Gastro-UrologyEZB1Manufactureraccessdata.fda.gov
Syringe, Restorative And Impression MaterialEID1Manufactureraccessdata.fda.gov
Unit, Syringe, Air And/Or WaterECB1Manufactureraccessdata.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
August 24, 2026K254286Guided Bone Regeneration SystemDZLSubstantially EquivalentDentalMaster(Xiamen)Medical Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated August 24, 2026. 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.