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Anhui Ares Medical Technology Co.,ltd.: FDA-registered device maker in Tianchang Anhui, China, 1 510(k) clearance

Anhui Ares Medical Technology Co.,ltd. is registered with the FDA (registration 3016426851) in Tianchang Anhui, China. It lists 28 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 17, 2024. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3016426851
Address
Yeshan Industrial Zone, Tianchang City, Anhui, China., Tianchang Anhui, China, 239300
Owner or operator
Anhui Ares Medical Technology Co.,Ltd. (10062137)
Roles
Contract manufacturer, Manufacturer
First device listed
December 22, 2019
Registered through
2026
Brand names listed
Air Water Syringe, EO indicator tapes, FLOSS, DENTAL, HVE TIPS, High Volume Evacuation (HVE) TIp, Non-surgical gown, UNIT, SYRINGE, AIR AND/OR WATER, Umbilical cord clamp and more

Devices it lists

DeviceProduct codeClassRoleSource
Absorber, Saliva, PaperKHR1Manufactureraccessdata.fda.gov
Accessory, Surgical ApparelLYU1Manufactureraccessdata.fda.gov
Apparatus, Suction, Single Patient Use, Portable, NonpoweredGCY1Manufactureraccessdata.fda.gov
Applicator, Absorbent Tipped, Non-SterileKXF1Manufactureraccessdata.fda.gov
Bag, Urine Collection, Leg, For External Use, Non-SterileNNW1Manufactureraccessdata.fda.gov
Bag, Urine Collection, Leg, For External Use, SterileFAQ1Contract manufacturer, Manufactureraccessdata.fda.gov
Bandage, ElasticFQM1Manufactureraccessdata.fda.gov
Cap, SurgicalFYF1Manufactureraccessdata.fda.gov
Catheter, Nasal, OxygenBZB1Manufactureraccessdata.fda.gov
Clamp, UmbilicalHFW2Manufactureraccessdata.fda.gov
Cotton, RollEFN1Manufactureraccessdata.fda.gov
Cover, Mattress (Medical Purposes)FMW1Manufactureraccessdata.fda.gov
Cup, ProphylaxisEHK1Manufactureraccessdata.fda.gov
Dress, SurgicalFYE1Manufactureraccessdata.fda.gov
Elastomer, Silicone, For Scar ManagementMDA1Manufactureraccessdata.fda.gov
Floss, DentalJES1Manufactureraccessdata.fda.gov
ForcepsHTD1Manufactureraccessdata.fda.gov
Forceps, Tooth Extractor, SurgicalEMG1Manufactureraccessdata.fda.gov
Gauze / Sponge,Nonresorbable For External UseNAB1Manufactureraccessdata.fda.gov
Indicator, Physical/Chemical Sterilization ProcessJOJ2Contract manufacturer, Manufactureraccessdata.fda.gov
Mask, SurgicalFXX2Contract manufactureraccessdata.fda.gov
Mirror, MouthEAX1Manufactureraccessdata.fda.gov
Mouthpiece, Saliva EjectorDYN1Manufactureraccessdata.fda.gov
Needle, Aspiration And Injection, DisposableGAA1Manufactureraccessdata.fda.gov
Non-Surgical GownOEA1Manufactureraccessdata.fda.gov
Shield, Protective, PersonnelKPY1Manufactureraccessdata.fda.gov
Unit, Syringe, Air And/Or WaterECB1Manufactureraccessdata.fda.gov
Wrap, SterilizationFRG2Contract 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 17, 2024K241036Autoclave Indicator Tape; EO Indicator TapeJOJSubstantially EquivalentJiangmen New Era External Use Drug Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated December 17, 2024. 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.