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Autoject Systems, Inc.

United StatesFDA applicant, unverified

Devices
4

What Autoject Systems, Inc. makes

Autoject Systems, Inc. manufactures electromyography (EMG) stimulators, including the AT33 EMG for muscle testing, and single-channel stimulators like the AT42 for nerve conduction studies. The company also produces the JECT-AID, a device for intramuscular injection assistance, and the AT64 SCR, a stimulator for skin conductance response testing.

These devices are classified as Class II under FDA regulations and are listed via the 510(k) clearance process. The company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue4

Newest first, rows 1-4 of 4

  • Ject-Aid Ref K853031

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

  • AT42 Ref K930576

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

  • AT33 Emg Ref K930578

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

  • AT64 Scr Ref K930577

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

Frequently asked questions

How many devices does Autoject Systems, Inc. have in the registry?

The registry currently lists 4 devices for Autoject Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Autoject Systems, Inc.'s devices?

Among its 4 most recently registered devices, Autoject Systems, Inc. has devices listed in FDA 510(k) (4 devices).

What risk classes do Autoject Systems, Inc.'s devices fall under?

Among its 4 most recently registered devices, the classes recorded for Autoject Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Autoject Systems, Inc. in the registry?

The most recently registered devices listed for Autoject Systems, Inc. include JECT-AID, AT42, AT33 EMG and AT64 SCR.

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