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Data / Medical devices / United States / Dental Evolutions, Inc

Dental Evolutions, Inc: FDA-registered device maker in Beverly Hills, CA, United States, 1 510(k) clearance

Dental Evolutions, Inc is registered with the FDA (registration 3012121192) in Beverly Hills, CA, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 27, 2015. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3012121192
Address
9100 Wilshire Blvd Ste 710W, Beverly Hills, CA, United States, 90212
Owner or operator
DENTAL EVOLUTIONS, INC (10050013)
Roles
Complaint file establishment, Specification developer
First device listed
October 5, 2015
Registered through
2026
Brand names listed
Implanova

Devices it lists

DeviceProduct codeClassRoleSource
Abutment, Implant, Dental, EndosseousNHA2Complaint file establishment, Specification developeraccessdata.fda.gov
Implant, Endosseous, Root-FormDZE2Complaint file establishment, 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
August 27, 2015K150040ImplanovaDZESubstantially EquivalentDental Evolutions, Inc.accessdata.fda.gov

Compare with other makers

Updated August 27, 2015. 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.