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I E Industries

Country not established

Devices
3

What I E Industries makes

I E Industries manufactures exam and manipulation tables along with procedure carts.

The company is based in the US, and its portfolio includes Class I and Class II devices that are listed in the FDA 510(k) registry.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

  • Table, Examination Ref K770437

    Class II
    Active 510(k) 510(k) II
  • Table, Exam & Manupulation Ref K770636

    Class I
    Active 510(k) 510(k) I
  • Cart, Procedures Ref K770438

    Class II
    Active 510(k) 510(k) II

Frequently asked questions

How many devices does I E Industries have in the registry?

The registry currently lists 3 devices for I E Industries. Devices recorded under merged duplicate company entries are counted once.

Which registries list I E Industries's devices?

Among its 3 most recently registered devices, I E Industries has devices listed in FDA 510(k) (3 devices).

What risk classes do I E Industries's devices fall under?

Among its 3 most recently registered devices, the classes recorded for I E Industries's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from I E Industries in the registry?

The most recently registered devices listed for I E Industries include TABLE, EXAMINATION, TABLE, EXAM & MANUPULATION and CART, PROCEDURES.

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