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Data / Medical devices / China / Unibeauty (hubei) Technology Co., Ltd.

Unibeauty (hubei) Technology Co., Ltd.: FDA-registered device maker in Xiantao Hubei, China, 4 510(k) clearances

Unibeauty (hubei) Technology Co., Ltd. is registered with the FDA (registration 3027520366) in Xiantao Hubei, China. It lists 1 device type. The FDA files 4 510(k) clearances under its listings, the newest dated December 17, 2025. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3027520366
Address
Building A8, nonwoven small and medium-sized enterprise Industrial Park, PENGCHANG Town, Xiantao Hubei, China, 433018
Owner or operator
Unibeauty (Hubei) Technology Co., Ltd. (10088143)
Roles
Exporter to the US, Manufacturer
First device listed
December 22, 2023
Registered through
2026
Brand names listed
L; R; S; SP, Unscented Menstrual Tampon

Devices it lists

DeviceProduct codeClassRoleSource
Tampon, Menstrual, UnscentedHEB2Exporter 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 17, 2025K253719Unscented Menstrual Long Applicator Tampon; Unscented Menstrual Cardboard Applicator Tampon; Unscented Menstrual Digital TamponsHEBSubstantially EquivalentUnibeauty (Hubei) Technology Co., Ltd.accessdata.fda.gov
September 19, 2025K252613Unscented menstrual three-piece applicator tamponHEBSubstantially EquivalentUnibeauty (Hubei) Technology Co., Ltd.accessdata.fda.gov
August 13, 2025K251033Unscented menstrual long applicator tampon; Unscented menstrual Compact Applicator Tampon; Unscented menstrual Cardboard Applicator Tampon; Unscented menstrual Digital TamponsHEBSubstantially EquivalentUnibeauty (Hubei) Technology Co., Ltd.accessdata.fda.gov
December 15, 2023K232598Unscented Menstrual TamponHEBSubstantially EquivalentUnibeauty (Hubei) Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated December 17, 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.