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Data / Medical devices / United States / Validic Logistics, LLC

Validic Logistics, LLC: FDA-registered device maker in Sterling, VA, United States, 6 510(k) clearances

Validic Logistics, LLC is registered with the FDA (registration 3027344406) in Sterling, VA, United States. It lists 4 device types. The FDA files 6 510(k) clearances under its listings, the newest dated April 20, 2017. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3027344406
Address
22626 Sally Ride Dr. Suite 110, Sterling, VA, United States, 20164
Owner or operator
Validic Logistics, LLC (10087999)
Roles
Repackager or relabeler
First device listed
May 12, 2023
Registered through
2026
Brand names listed
A&D Blood Pressure Monitor, ChoiceMMed MD800, ForaCare IR20b v4, Nonin Pulse Oximeter, Omron HEM-9200T, Omron HEM-9210T

Devices it lists

DeviceProduct codeClassRoleSource
Continuous Measurement ThermometerFLL2Repackager or relabeleraccessdata.fda.gov
Monitor, Ultrasonic, FetalKNG2Repackager or relabeleraccessdata.fda.gov
OximeterDQA2Repackager or relabeleraccessdata.fda.gov
System, Measurement, Blood-Pressure, Non-InvasiveDXN2Repackager or relabeleraccessdata.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
April 20, 2017K163235HEM-9210TDXNSubstantially EquivalentOmron Healthcare, Inc.accessdata.fda.gov
October 7, 2014K141160A&D MEDICAL UA-651 DIGITAL BLOOD PRESSURE MONITORDXNSubstantially EquivalentA & D Co., Ltd.accessdata.fda.gov
January 16, 2014K133379HEM-7311DXNSubstantially EquivalentOmron Healthcare, Inc.accessdata.fda.gov
September 11, 2013K131021PULSE OXIMETERDQASubstantially EquivalentNonin Medical, Inc.accessdata.fda.gov
October 27, 2011K112911FETAL DOPPLERKNGSubstantially EquivalentBeijing Choice Electronic Technololgy Co., Ltd.accessdata.fda.gov
March 10, 2009K090395FORA IR20B EAR THERMOMETER, MODEL TD-1261F, FORA IR21B EAR THERMOMETER, MODEL TD-1261EFLLSubstantially EquivalentTaidoc Technology Corporationaccessdata.fda.gov

Compare with other makers

Updated April 20, 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.