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Ritract, Ltd.

AustraliaFDA applicant, unverified

Devices
1

What Ritract, Ltd. makes

Ritract, Ltd. manufactures the Ritract Safety Syringe, a pre-filled, single-use syringe designed to reduce needle-stick injuries through a retractable needle mechanism.

The company’s product portfolio is regulated under FDA Class II devices and is listed via the 510(k) clearance process. The manufacturer is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Ritract Safety Syringe Ref K060002

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

Frequently asked questions

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

The registry currently lists 1 device for Ritract, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Ritract, Ltd.'s devices?

Among its 1 most recently registered device, Ritract, Ltd. has devices listed in FDA 510(k) (1 device).

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

Among its 1 most recently registered device, the classes recorded for Ritract, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Ritract, Ltd. include RITRACT SAFETY SYRINGE.

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