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Qed, Inc.

United Statesfrom the FDA registration address FDA FEI 1037039

Qed, Inc. is a medical device manufacturer, with 8 devices listed in FDA GUDID (FDA Class II and I) as of 13 Nov 2026.

Devices
8
Registrations
FDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • FDA GUDID 8
Device classes
  • FDA Class II 5
  • FDA Class I 3
Identifiers
  • FDA FEI 1037039
  • DUNS 877534289

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

Catalogue8

Newest first, rows 1-8 of 8

Company details

FDA FEI number
1037039
DUNS number
877534289
Address
750 ENTERPRISE DR., LEXINGTON, KY, 40510
Phone
859-231-0338

Frequently asked questions

How many devices does QED, INC. have in the registry?

The registry currently lists 8 devices for QED, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list QED, INC.'s devices?

Among its 8 most recently registered devices, QED, INC. has devices listed in FDA GUDID (8 devices).

What risk classes do QED, INC.'s devices fall under?

Among its 8 most recently registered devices, the classes recorded for QED, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from QED, INC. in the registry?

The most recently registered devices listed for QED, INC. include Nova 3 QED-2050, Nova 300 QED-3010, Altair HI 2 QED-7800 and EOS QED-4604.

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