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Woundvision, LLC

United Statesfrom the FDA registration address FDA FEI 3010696641

Devices
1
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

What Woundvision, LLC makes

Woundvision, LLC manufactures wound measuring and monitoring devices designed to assess and track wound dimensions and healing progress for clinical use.

These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. 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

Company details

FDA FEI number
3010696641
Address
10585 North Meridian St., Indianapolis, IN, 46290

Frequently asked questions

How many devices does Woundvision, LLC have in the registry?

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

Which registries list Woundvision, LLC's devices?

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

What risk classes do Woundvision, LLC's devices fall under?

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

What are the newest devices from Woundvision, LLC in the registry?

The most recently registered devices listed for Woundvision, LLC include WOUND MEASURING & MONITORING DEVICE.

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