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InnovaCorium, Inc.

United Statesfrom the FDA registration address FDA FEI 3018161300

Devices
1
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

What InnovaCorium, Inc. makes

InnovaCorium, Inc. manufactures the IWD-Gel™, a medical device designed for intravascular use, likely intended for wound care or vascular applications within blood vessels.

The IWD-Gel™ is classified as a Class II (U) 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, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • IWD-Gel™ Ref K254191

    Active Regimes: 510(k) Registry: 510(k) Class:—

Company details

FDA FEI number
3018161300
Address
747 Sw 2nd Ave Ste 354, Gainesville, FL, 32601

Frequently asked questions

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

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

Which registries list InnovaCorium, Inc.'s devices?

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

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

The most recently registered devices listed for InnovaCorium, Inc. include IWD-Gel™.

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