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A&D Engineering, Inc.

Country not established FDA establishment FEI 1000110823

Devices
34
Registrations
FDA
FDA recalls
0

Catalogue34

Newest first, rows 1-34 of 34

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Rows 1-34 of 34

Company details

FDA FEI number
1000110823
Address
2605 N.Berkeley Lake Rd., Duluth, GA, 30096

Frequently asked questions

How many devices does A&D Engineering, Inc. have in the registry?

The registry currently lists 34 devices for A&D Engineering, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list A&D Engineering, Inc.'s devices?

Among its 34 most recently registered devices, A&D Engineering, Inc. has devices listed in FDA 510(k) (34 devices).

What risk classes do A&D Engineering, Inc.'s devices fall under?

Among its 34 most recently registered devices, the classes recorded for A&D Engineering, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from A&D Engineering, Inc. in the registry?

The most recently registered devices listed for A&D Engineering, Inc. include A & D UB-302 WRIST DIGITAL BLOOD PRESSURE MONITOR, DIGITAL BLOOD PRESSURE MONITORS, MODELS TM-2655, TM-2655P, & TM-2655VP, A&D MEDICAL LIFESOURCE DIGITAL BLOOD PRESSURE MONITORS, MODELS UB-511 & UB-512 and A & D MEDICAL UA-767BT DIGITAL BLOOD PRESSURE MONITOR.

Generated automatically from registry data and not verified by a human reviewer.

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.