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Data / Medical devices / United States / Inventeur, LLC

Inventeur, LLC: FDA-registered device maker in Saint Petersburg, FL, United States, 1 510(k) clearance

Inventeur, LLC is registered with the FDA (registration 3038913749) in Saint Petersburg, FL, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 16, 2024. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3038913749
Address
7901 4th St N Ste 300, Saint Petersburg, FL, United States, 33702
Owner or operator
Inventeur, LLC (10093634)
Roles
Specification developer
First device listed
June 15, 2025
Registered through
2026
Brand names listed
Anesthesia Intraoral Module (AIM)

Devices it lists

DeviceProduct codeClassRoleSource
Analyzer, Gas, Carbon-Dioxide, Gaseous-PhaseCCK2Specification developeraccessdata.fda.gov
Cannula, Nasal, OxygenCAT1Specification developeraccessdata.fda.gov
Endoscopic Bite BlockMNK1Specification 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
December 16, 2024K240937AIM (N/A)CCKSubstantially EquivalentInventeur, LLCaccessdata.fda.gov

Compare with other makers

Updated December 16, 2024. 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.