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Data / Medical devices / United States / Ibl Acquisitions LLC

Ibl Acquisitions LLC: FDA-registered device maker in Indianapolis, IN, United States, 3 510(k) clearances

Ibl Acquisitions LLC is registered with the FDA (registration 3008799671) in Indianapolis, IN, United States. It lists 1 device type. The FDA files 3 510(k) clearances under its listings, the newest dated July 6, 2017. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3008799671
Address
5650 Elmwood Ave, Indianapolis, IN, United States, 46203
Owner or operator
IBL Acquisitions LLC (10044810)
Roles
Complaint file establishment, Manufacturer, Specification developer
First device listed
February 27, 2020
Registered through
2026
Brand names listed
IBL 5000 Tanning Booth, Mastersun 360, SunFit Replacement Lamps

Devices it lists

DeviceProduct codeClassRoleSource
Booth, Sun TanLEJ2Complaint file establishment, Manufacturer, 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
July 6, 2017K161394HPO Exotic, LP1, LP2, LP3, Mastersun 360, Mastersun 360 New Reflector, Vega LuxLEJSubstantially EquivalentSportarredo Group S.C.accessdata.fda.gov
September 1, 2016K152405IBL 5000 Tanning BoothLEJSubstantially EquivalentIbl Acquisitions, LLCaccessdata.fda.gov
January 27, 2016K152233BPhase, HPO Exotic, LPI, LP2, LP3, Mastersun 360, Mastersun 360 New Reflector, Vega LuxLEJSubstantially EquivalentSportarredo Group S.C.accessdata.fda.gov

Compare with other makers

Updated July 6, 2017. 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.