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King-Devick Technologies, Inc

Country not established FDA establishment FEI 3017858031

Devices
1
Registrations
FDA
FDA recalls
0

Catalogue1

Newest first, rows 1-1 of 1

  • K-D Balance Ref K173669

    Unclassified
    Active 510(k) 510(k) —

Company details

FDA FEI number
3017858031
Address
2150 McDonald Drive Unit 1120, Oak Brook, IL, 60523

Frequently asked questions

How many devices does KING-DEVICK TECHNOLOGIES, INC have in the registry?

The registry currently lists 1 device for KING-DEVICK TECHNOLOGIES, INC. Devices recorded under merged duplicate company entries are counted once.

Which registries list KING-DEVICK TECHNOLOGIES, INC's devices?

Among its 1 most recently registered device, KING-DEVICK TECHNOLOGIES, INC has devices listed in FDA 510(k) (1 device).

What are the newest devices from KING-DEVICK TECHNOLOGIES, INC in the registry?

The most recently registered devices listed for KING-DEVICK TECHNOLOGIES, INC include K-D Balance.

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.