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Data / Medical devices / United States / Specialty Water Technologies, Inc.

Specialty Water Technologies, Inc.: FDA-registered device maker in Portland, TN, United States, 2 510(k) clearances

Specialty Water Technologies, Inc. is registered with the FDA (registration 3012119281) in Portland, TN, United States. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated March 17, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3012119281
Address
104 Flex Ave, Portland, TN, United States, 37148
Owner or operator
Specialty Water Technologies, Inc. (10050005)
Roles
Manufacturer
First device listed
October 5, 2015
Registered through
2026
Brand names listed
UPT Series Medical RO Water System

Devices it lists

DeviceProduct codeClassRoleSource
Subsystem, Water PurificationFIP2Manufactureraccessdata.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
March 17, 2025K250514UPT Series Medical RO Water Treatment SystemFIPSubstantially EquivalentSpecialty Water Technologies, Inc.accessdata.fda.gov
September 23, 2015K151637UPT Series Medical RO Water SystemFIPSubstantially EquivalentSpecialty Water Technologiesaccessdata.fda.gov

Compare with other makers

Updated March 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.