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Data / Medical devices / United States / United Service Solutions, LLC

United Service Solutions, LLC: FDA-registered device maker in Westborough, MA, United States, 1 510(k) clearance

United Service Solutions, LLC is registered with the FDA (registration 3014640847) in Westborough, MA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 30, 2008. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3014640847
FEI number
3003300201
Address
1700 West Park Drive, Westborough, MA, United States, 01581
Owner or operator
United Service Solutions, LLC (10057910)
Roles
Specification developer
First device listed
June 12, 2018
Registered through
2026
Brand names listed
Piezolith 3000 Triple Focus

Devices it lists

DeviceProduct codeClassRoleSource
Lithotriptor, Extracorporeal Shock-Wave, UrologicalLNS2Specification 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
January 30, 2008K072538PIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPTERLNSSubstantially EquivalentUnited Medical Systems, Inc.accessdata.fda.gov

Compare with other makers

Updated January 30, 2008. 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.