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Bio-Vascular, Inc.

United StatesFDA applicant, unverified

Devices
26

What Bio-Vascular, Inc. makes

Bio-Vascular, Inc. manufactures tissue-based medical devices, including pericardial and dural patches, vessel occluders, and reinforcement strips for surgical staple lines. Their products also cover tissue grafts and specialized barriers like the Dura-Guard dural repair patch and FLO-Rester disposable vessel occluder. Additional offerings include diagnostic tools such as the Advanced Diagnostic Viewer (ADV) and sling implants for medical applications.

The company’s portfolio includes devices classified under FDA’s Class I and Class II categories, with most products subject to 510(k) clearance. These devices are listed in the FDA’s 510(k) registry, reflecting their regulatory status in the United States. The manufacturer operates from the US.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does Bio-Vascular, Inc. have in the registry?

The registry currently lists 26 devices for Bio-Vascular, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Bio-Vascular, Inc.'s devices?

Among its 26 most recently registered devices, Bio-Vascular, Inc. has devices listed in FDA 510(k) (26 devices).

What risk classes do Bio-Vascular, Inc.'s devices fall under?

Among its 26 most recently registered devices, the classes recorded for Bio-Vascular, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Bio-Vascular, Inc. in the registry?

The most recently registered devices listed for Bio-Vascular, Inc. include TISSUE PATCH, TISSUE GRAFT, PERI-STRIPS DRY - STAPLE LINE REINFORCEMENT, VASCU-GUARD and BVI SLING.

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