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Boston-Biomedical Associates

Country not established

Devices
1

What Boston-Biomedical Associates makes

Boston-Biomedical Associates manufactures the Aegis Transit System, a medical device designed for vascular access and catheter insertion, intended to reduce complications during procedures.

The Aegis Transit System is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company 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

  • Aegis Transit System Ref K170757

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

Frequently asked questions

How many devices does Boston-Biomedical Associates have in the registry?

The registry currently lists 1 device for Boston-Biomedical Associates. Devices recorded under merged duplicate company entries are counted once.

Which registries list Boston-Biomedical Associates's devices?

Among its 1 most recently registered device, Boston-Biomedical Associates has devices listed in FDA 510(k) (1 device).

What risk classes do Boston-Biomedical Associates's devices fall under?

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

What are the newest devices from Boston-Biomedical Associates in the registry?

The most recently registered devices listed for Boston-Biomedical Associates include Aegis Transit System.

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