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Convatec, A Division of E.R. Squibb & Sons

Also registered as Convatec, A Division of E.R. Squibb & Sons, LLC

Country not established

Devices
84

What Convatec, A Division of E.R. Squibb & Sons makes

The company manufactures wound care and stoma management products, including hydrocolloid dressings (such as DUODERM and DUODERM EXTRA THIN), adhesive compression bandages, sterile skin barriers, and odor control wound dressings. It also produces absorbent pads for incontinence care, nonwoven pads, dermatological patches, and stoma-related barrier wipes and systems.

These products are regulated under FDA classifications including Class I, Class II, and Unclassified (U), with many cleared via the 510(k) pathway. The company’s devices are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does Convatec, A Division of E.R. Squibb & Sons have in the registry?

The registry currently lists 84 devices for Convatec, A Division of E.R. Squibb & Sons. Devices recorded under merged duplicate company entries are counted once.

Which registries list Convatec, A Division of E.R. Squibb & Sons's devices?

Among its 50 most recently registered devices, Convatec, A Division of E.R. Squibb & Sons has devices listed in FDA 510(k) (50 devices).

What risk classes do Convatec, A Division of E.R. Squibb & Sons's devices fall under?

Among its 50 most recently registered devices, the classes recorded for Convatec, A Division of E.R. Squibb & Sons's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Convatec, A Division of E.R. Squibb & Sons in the registry?

The most recently registered devices listed for Convatec, A Division of E.R. Squibb & Sons include DUODERM(R) ADHESIVE COMPRESSION BANDAGE, MODIFIED, DUODERM DRESSINGS, CGF DRESSINGS, PASTE FULL THICK, STOMAHESIVE SKIN BARRIER STERILE and ALLKARE BARRIER WIPE.

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