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Vitaphore Corp.

United StatesFDA 510(k) applicant, unverified

Devices
13

What Vitaphore Corp. makes

Vitaphore Corp. manufactures wound care dressings, including collagen-based sponges and silver foam dressings, as well as antimicrobial catheter securement devices. Their product line also includes catheter introducer systems and kits, percutaneous pin protection devices, and infection control kits for percutaneous procedures. Collagen-based shields for acute care settings are part of their portfolio, designed to support tissue healing and reduce infection risk.

The company’s devices are classified under FDA categories Class I, Class II, and Unclassified (U), with most submissions supported by 510(k) clearances. Their products are listed in the FDA’s 510(k) database, reflecting regulatory compliance for medical devices in the United States.

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 Vitaphore Corp. have in the registry?

The registry currently lists 13 devices for Vitaphore Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Vitaphore Corp.'s devices?

Among its 13 most recently registered devices, Vitaphore Corp. has devices listed in FDA 510(k) (13 devices).

What risk classes do Vitaphore Corp.'s devices fall under?

Among its 13 most recently registered devices, the classes recorded for Vitaphore Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Vitaphore Corp. in the registry?

The most recently registered devices listed for Vitaphore Corp. include VITACHOICE WOUND DRESSING, VITAACCESS (TM) CATHETER INTRODUCER SYSTEM, VITAACCESS CATHETER INTRODUCER KIT and VITAPATCH CATH. SECUREMENT DEVICE W/CHLORHEXIDINE.

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