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Data / Medical devices / United States / Lares Research

Lares Research: FDA-registered device maker in Chico, CA, United States, 7 510(k) clearances

Lares Research is registered with the FDA (registration 2916440) in Chico, CA, United States. It lists 7 device types. The FDA files 7 510(k) clearances under its listings, the newest dated December 15, 2022. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
2916440
Address
295 Lockheed Ave, Chico, CA, United States, 95973
Owner or operator
LARES RESEARCH (2916440)
Roles
Manufacturer, Remanufacturer, Repackager or relabeler
First device listed
November 12, 1992
Registered through
2026
Brand names listed
557 ProStyle SF Lite 2H, 557 ProStyle SF Lite 4H C, 557 ProStyle SF Lite 4H LC, 557 ProStyle SF Lite NSK SC, 557 ProStyle SF Lite NSK SLC, 557 ProStyle SF Lite SC, 557 ProStyle SF Lite SLC, 557 ProStyle SF NSK SC and more

Devices it lists

DeviceProduct codeClassRoleSource
Agent, Polishing, Abrasive, Oral CavityEJR1Repackager or relabeleraccessdata.fda.gov
Bur, DentalEJL1Repackager or relabeleraccessdata.fda.gov
Handpiece, Air-Powered, DentalEFB1Manufacturer, Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Handpiece, Belt And/Or Gear Driven, DentalEFA1Repackager or relabeleraccessdata.fda.gov
Handpiece, Contra- And Right-Angle Attachment, DentalEGS1Manufacturer, Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Instrument, Diamond, DentalDZP1Repackager or relabeleraccessdata.fda.gov
Unit, Operative DentalEIA1Manufactureraccessdata.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 15, 2022K220873Perceptive electric dental motor and control unitEIASubstantially EquivalentLares Researchaccessdata.fda.gov
November 7, 2022K220874Smooth Drive contra angle and straight handpiecesEGSSubstantially EquivalentLares Researchaccessdata.fda.gov
September 3, 2021K202786Dental Low-speed Handpieces and AccessoriesEFBSubstantially EquivalentMicrop Technology (Taiwan), Inc.accessdata.fda.gov
October 28, 2014K141221LARES ULTRALITE PROSTYLE HIGH-SPEED DENTAL HANDPIECES, LARES EURO PROSTYLE HIGH-SPEED DENTAL HANDPIECES, LARES TURBO+ PREFBSubstantially EquivalentLares Research, Inc.accessdata.fda.gov
March 20, 2008K073652ND LOW SPEED AIRMOTOR AND HANDPIECE, HIGHSPEED AIRTURBINE HANDPIECE, E-TYPE STRAIGHT NOSECONE AND CONTRA ANGLEEFBSubstantially EquivalentNakamura Magnifier Co., Ltd.accessdata.fda.gov
October 9, 1997K973062TWIST RECIPROCATING DISPOSABLE PROPHY ANGLEEFASubstantially EquivalentMedidenta Intl., Inc.accessdata.fda.gov
April 23, 1996K961163LARES RESEARCH AS-1 LOWSPEED HANDPIECEEFBSubstantially EquivalentLares Research, Inc.accessdata.fda.gov

Compare with other makers

Updated December 15, 2022. 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.