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Medical Plastics, Inc.

United StatesFDA applicant, unverified

Devices
7

What Medical Plastics, Inc. makes

Medical Plastics, Inc. manufactures surgical drapes, including abdominal and C-section drape sheets, designed for sterile field protection during procedures. The company also produces electrosurgical tools, such as the electrosurgical pencil system and a capacitive dispersive pad, which manage electrical current during tissue ablation. Additionally, it supplies the MON-IT II smart safety system, a monitoring device for electrosurgical procedures to enhance patient safety.

The company’s products are classified as Class II medical devices under FDA regulations and are listed in the 510(k) clearance registry. These devices are intended for use in surgical and procedural settings in the United States, adhering to federal requirements for electrosurgical and sterile barrier products.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue7

Newest first, rows 1-7 of 7

Frequently asked questions

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

The registry currently lists 7 devices for Medical Plastics, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Medical Plastics, Inc.'s devices?

Among its 7 most recently registered devices, Medical Plastics, Inc. has devices listed in FDA 510(k) (7 devices).

What risk classes do Medical Plastics, Inc.'s devices fall under?

Among its 7 most recently registered devices, the classes recorded for Medical Plastics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Medical Plastics, Inc. include FEMORAL ANGIOGRAPHY DRAPE, UNDER BUTTOCKS DRAPE, ABDOMINAL OR C-SECTION DRAPE SHEET and ELECTROSURGICAL PENCIL SYSTEM.

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