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Data / Medical devices / United States / HTT Technologies Inc.

HTT Technologies Inc.: FDA-registered device maker in Bentonville, AR, United States, 1 510(k) clearance

HTT Technologies Inc. is registered with the FDA (registration 3038179167) in Bentonville, AR, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 13, 2019. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3038179167
Address
820 S Walton Blvd Ste 17, Bentonville, AR, United States, 72712
Owner or operator
HTT Technologies Inc. (10093294)
Roles
Repackager or relabeler, Specification developer
First device listed
April 25, 2025
Registered through
2026

Devices it lists

DeviceProduct codeClassRoleSource
Bandage, ElasticFQM1Repackager or relabeleraccessdata.fda.gov
Dressing, Wound, DrugFROURepackager or relabeleraccessdata.fda.gov
Tape And Bandage, AdhesiveKGX1Repackager or relabeler, Specification developeraccessdata.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
September 13, 2019K181478Roosin Xeroform Petrolatum DressingFROSubstantially EquivalentRoosin Medical Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated September 13, 2019. 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.