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Data / Medical devices / United States / A and D Engineering, Inc.

A and D Engineering, Inc.: FDA-registered device maker in Hoschton, GA, United States, 16 510(k) clearances

A and D Engineering, Inc. is registered with the FDA (registration 3044174020) in Hoschton, GA, United States. It lists 6 device types. The FDA files 16 510(k) clearances under its listings, the newest dated April 24, 2019. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number
3044174020
Address
1075 Highway 124W Building 400, Suite 150, Hoschton, GA, United States, 30548
Owner or operator
A&D Company, Limited (8031633)
Roles
Contract manufacturer, Repackager or relabeler
First device listed
September 9, 2005
Registered through
2027
Brand names listed
A&D Medical UB-543, A&D Medical UM-211 Digital Blood Pressure Monitor, DT-102, DT-103, DT-105 Thermometer, Digital Blood Pressure Monitor, System, Measurement, Blood Pressure Non-invasive, TM-2440 & TM-2441 and more

Devices it lists

DeviceProduct codeClassRoleSource
Analyzer, Body Composition, ExemptPUH2Repackager or relabeleraccessdata.fda.gov
Blood Pressure CuffDXQ2Contract manufactureraccessdata.fda.gov
Continuous Measurement ThermometerFLL2Repackager or relabeleraccessdata.fda.gov
Scale, PatientFRW1Repackager or relabeleraccessdata.fda.gov
Scale, Stand-On, PatientFRI1Repackager or relabeleraccessdata.fda.gov
System, Measurement, Blood-Pressure, Non-InvasiveDXN2Contract manufacturer, Repackager 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 24, 2019K173065A&D Medical Blood Pressure MonitorsDXNSubstantially EquivalentA&D Company, Ltd.accessdata.fda.gov
March 21, 2019K173191A&D Medical Blood Pressure MonitorsDXNSubstantially EquivalentA&D Company, Ltd.accessdata.fda.gov
September 19, 2017K163518Digital ThermometerFLLSubstantially EquivalentJoytech Healthcare Co. , Ltd.accessdata.fda.gov
May 17, 2017K170196A&D Medical UB-1100BLE UltraConnect Digital Blood Pressure MonitorDXNSubstantially EquivalentA&D Company, Ltd.accessdata.fda.gov
April 13, 2016K151953A&D Medical TM-2657 Family of Digital Blood Pressure MonitorsDXNSubstantially EquivalentA&D Company, Ltd.accessdata.fda.gov
October 8, 2014K141201A&D MEDICAL UA-767F AND UA-767FAC DIGITAL BLOOD PRESSURE MONITORDXNSubstantially EquivalentA & D Co., Ltd.accessdata.fda.gov
October 7, 2014K141160A&D MEDICAL UA-651 DIGITAL BLOOD PRESSURE MONITORDXNSubstantially EquivalentA & D Co., Ltd.accessdata.fda.gov
June 27, 2014K141179A&D MEDICAL UB-543 DIGITAL BLOOD PRESSURE MONITORDXNSubstantially EquivalentA & D Co., Ltd.accessdata.fda.gov
August 1, 2011K111686A & D MEDICAL UA-1000 FAMILY DAGITAL BLOOD PRESSURE MONITORSDXNSubstantially EquivalentA&D Company, Ltd.accessdata.fda.gov
January 7, 2010K092447DIGITAL THERMOMETER (WITH DISPOSABLE THERMOMETER COVER), DT SERIESFLLSubstantially EquivalentHangzhou Hua'An Medical & Health Instruments Co.,accessdata.fda.gov
January 19, 2007K062027A&D MEDICAL UA-789 DIGITAL BLOOD PRESSURE MONITORDXNSubstantially EquivalentA&D Engineering, Inc.accessdata.fda.gov
March 3, 2005K043217A&D MEDICAL UA-767PBT DIGITAL BLOOD PRESSURE MONITORDXNSubstantially EquivalentA&D Engineering, Inc.accessdata.fda.gov
December 3, 2004K042967A&D MEDICAL LIFESOURCE DIGITAL BLOOD PRESSURE MONITORS, MODELS UB-511 & UB-512DXNSubstantially EquivalentA&D Engineering, Inc.accessdata.fda.gov
October 30, 2003K032499A & D MEDICAL LIFESOURCE UA-704 DIGITAL BLOOD PRESSURE MONITORSDXNSubstantially EquivalentA&D Engineering, Inc.accessdata.fda.gov
February 15, 2002K012472A & D MEDICAL LIFESOURCE UA-781, UA781PC, & UA-781T DIGITAL BLOOD PRESSURE MONITORSDXNSubstantially EquivalentA&D Engineering, Inc.accessdata.fda.gov
December 29, 2000K002182AVITA TSO/TS1 INFRARED EAR THERMOMETERFLLSubstantially EquivalentAvita Corporationaccessdata.fda.gov

Compare with other makers

Updated April 24, 2019. 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.