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Promamedical, Inc.

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Devices
1

What Promamedical, Inc. makes

Promamedical, Inc. manufactures a range of hypodermic needles under the MESORAM® brand, including variants for different gauges, lengths, and applications such as insulin delivery, blood collection, and general injections.

These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States and its products are listed in the FDA’s 510(k) registry.

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

Catalogue1

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Frequently asked questions

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

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

Which registries list Promamedical, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Promamedical, Inc. include MESORAM® Hypodermic Needle (710301); MESORAM® Hypodermic Needle (710302); MESORAM® Hypodermic Needle (712305); MESORAM® Hypodermic Needle (712315); MESORAM® Hypodermic Needle (710303); MESORAM® Hypodermic Needle (710307); MESORAM® Hypodermic Needle (710306); MESORAM® Hypodermic Needle (712308); MESORAM® Hypodermic Needle (712318); MESORAM® Hypodermic Needle (712303); MESORAM® Hypodermic Needle (712307); MESORAM® Hypodermic Needle (712306); MESORAM® Hypodermic Needle (812400); MESORAM®.

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