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Data / Medical devices / United States / Novaerus Us Inc.

Novaerus Us Inc.: FDA-registered device maker in Charlotte, NC, United States, 1 510(k) clearance

Novaerus Us Inc. is registered with the FDA (registration 3019543795) in Charlotte, NC, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 28, 2020. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3019543795
Address
3540 Toringdon Way Ste 200, Charlotte, NC, United States, 28277
Owner or operator
Novaerus US Inc. (10082124)
Roles
Specification developer
First device listed
June 17, 2021
Registered through
2026
Brand names listed
Novaerus Defend 1050, Novaerus Defend 400, Novaerus NV1050, Novaerus NV400, Novaerus Pro XL, WellAir Defend 1050, WellAir Defend 400, WellAir NV1050 and more

Devices it lists

DeviceProduct codeClassRoleSource
Cleaner, Air, Medical RecirculatingFRF2Specification 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 28, 2020K200321Novaerus NV1050FRFSubstantially EquivalentNovaerus Us, Inc.accessdata.fda.gov

Compare with other makers

Updated December 28, 2020. 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.