Skip to content

Researched, Novel Medical Devices (Rn/Md)

Country not established

Devices
3

What Researched, Novel Medical Devices (Rn/Md) makes

The company produces single-use specimen collection and transport containers for laboratory samples, including sealed containers designed for safe handling and transport. It also manufactures split-top wing needle caps with optional tubing anchors and compatible recap devices to improve needle safety and workflow. Additionally, it offers bedside caddies for organizing and storing medical supplies at patient care locations.

The portfolio includes devices classified as Class I and Class II under FDA regulations, with submissions supported via the 510(k) pathway. These products are listed in the FDA’s 510(k) database. The company is based in the United States.

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

Catalogue3

Newest first, rows 1-3 of 3

Frequently asked questions

How many devices does Researched, Novel Medical Devices (Rn/Md) have in the registry?

The registry currently lists 3 devices for Researched, Novel Medical Devices (Rn/Md). Devices recorded under merged duplicate company entries are counted once.

Which registries list Researched, Novel Medical Devices (Rn/Md)'s devices?

Among its 3 most recently registered devices, Researched, Novel Medical Devices (Rn/Md) has devices listed in FDA 510(k) (3 devices).

What risk classes do Researched, Novel Medical Devices (Rn/Md)'s devices fall under?

Among its 3 most recently registered devices, the classes recorded for Researched, Novel Medical Devices (Rn/Md)'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Researched, Novel Medical Devices (Rn/Md) in the registry?

The most recently registered devices listed for Researched, Novel Medical Devices (Rn/Md) include ONE STEP SPECIMEN COLLECTOR/TRANSPORT CONTAINER, SPLIT TOP WING NEEDLE CAP WITH OPTIONAL TUBING ANCHORS (AND APPROPRIATE RECAP DEVICE and BEDSIDE CADDY.

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