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Inteware Co., Ltd.

ChinaFDA applicant, unverified FDA

Devices
2
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA establishment

Catalogue2

Newest first, rows 1-2 of 2

  • OrthoAnalysis Software Ref K183695

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Implant Planning Software Ref K173965

    Active Regimes: 510(k) Registry: 510(k) Class:II

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Inteware Co., Ltd Chiayi County Chiayi(County) · TW FEI 3013912897

Frequently asked questions

How many devices does Inteware Co., Ltd. have in the registry?

The registry currently lists 2 devices for Inteware Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Inteware Co., Ltd.'s devices?

Among its 2 most recently registered devices, Inteware Co., Ltd. has devices listed in FDA 510(k) (2 devices).

What risk classes do Inteware Co., Ltd.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Inteware Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Inteware Co., Ltd. in the registry?

The most recently registered devices listed for Inteware Co., Ltd. include OrthoAnalysis Software and Implant Planning Software.

Which FDA establishments are linked to Inteware Co., Ltd.?

1 FDA establishment is linked to Inteware Co., Ltd. in the registry; they are listed on the company page.

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