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Merocel Corp.

United StatesFDA applicant, unverified

Devices
10

What Merocel Corp. makes

Merocel Corp. manufactures wound care dressings, including absorbent and reinforced silicone sheets for skin protection, as well as hemostatic dressings designed to control bleeding. Their portfolio also includes nasal and septal medical devices, such as turbinate gloves, septal splints, and epistaxis kits for nasal bleeding management. Additional products include laser protection shields for medical procedures, vaginal packs, and nasal catheters for drainage.

The company’s devices are regulated under FDA classifications, including Class I, Class II, and Unclassified (U) devices, with many authorised via the 510(k) pathway. Products are listed in the FDA’s 510(k) database, and the company operates from the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue10

Newest first, rows 1-10 of 10

Frequently asked questions

How many devices does Merocel Corp. have in the registry?

The registry currently lists 10 devices for Merocel Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Merocel Corp.'s devices?

Among its 10 most recently registered devices, Merocel Corp. has devices listed in FDA 510(k) (10 devices).

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

Among its 10 most recently registered devices, the classes recorded for Merocel Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Merocel Corp. include MEROCEL WOUND DRESSING, MEROCEL REINFORCED SILICONE SHEETS, MEROCEL(R) WOUND DRESSING (WITH HEMOSTATIC CLAIM) and MEROCEL(R) TURBINATE GLOVE AND SEPTAL SPLINT.

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