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Htt Technologies Inc.

United Statesfrom the FDA registration address FDA establishment FEI 3038179167

Devices
9
Registrations
FDA
FDA recalls
0

Catalogue9

Newest first, rows 1-9 of 9

  • Oktape 4003-A2

    Withdrawn Registry: GUDID Class:I

  • Oktape 4003-A1

    Withdrawn Registry: GUDID Class:I

  • Oktape 4003-A0

    Withdrawn Registry: GUDID Class:I

  • Oktape 4004-A2

    Withdrawn Registry: GUDID Class:I

  • Oktape 4004-A3

    Withdrawn Registry: GUDID Class:I

  • Oktape 6211-Bw

    Withdrawn Registry: GUDID Class:I

  • Oktape 6211-Rd

    Withdrawn Registry: GUDID Class:I

  • Oktape 6229-LBU2

    Withdrawn Registry: GUDID Class:I

  • Oktape 6211-Gn

    Withdrawn Registry: GUDID Class:I

Company details

FDA FEI number
3038179167
Address
820 S Walton Blvd Ste 17, Bentonville, AR, 72712

Frequently asked questions

How many devices does HTT TECHNOLOGIES INC. have in the registry?

The registry currently lists 9 devices for HTT TECHNOLOGIES INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list HTT TECHNOLOGIES INC.'s devices?

Among its 9 most recently registered devices, HTT TECHNOLOGIES INC. has devices listed in FDA GUDID (9 devices).

What risk classes do HTT TECHNOLOGIES INC.'s devices fall under?

Among its 9 most recently registered devices, the classes recorded for HTT TECHNOLOGIES INC.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from HTT TECHNOLOGIES INC. in the registry?

The most recently registered devices listed for HTT TECHNOLOGIES INC. include OKTAPE 4003-A2, OKTAPE 4003-A1, OKTAPE 4003-A0 and OKTAPE 4004-A2.

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.