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Clearmedical, Inc.

United StatesFDA applicant, unverified

Devices
14

What Clearmedical, Inc. makes

Clearmedical, Inc. manufactures reprocessed single-use medical devices including surgical scissors and graspers, trocars, reloadable cutters, staplers, appliers, multiple clip appliers, and biopsy forceps. The company also produces blood pressure cuffs under the Clearmedical/Critikon and Clearmedical/Welch Allyn brands, foot garments such as Huntleigh models FG200 and FG100 in various sizes, knee-high and thigh-high SCD sleeves from Kendall, DVT garments, Venaflow calf and thigh cuffs from Aircast, and Nellcor Oxisensor II pulse oximetry sensors for adult and neonatal use.

The devices in Clearmedical, Inc.'s portfolio are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.

AI-generated from registry data, 29 Sep 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

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

The registry currently lists 14 devices for Clearmedical, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Clearmedical, Inc.'s devices?

Among its 14 most recently registered devices, Clearmedical, Inc. has devices listed in FDA 510(k) (14 devices).

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

Among its 14 most recently registered devices, the classes recorded for Clearmedical, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Clearmedical, Inc. include CLEARMEDICAL/CRITIKON BLOOD PRESSURE CUFF; CLEARMEDICAL/WELCH ALLYN BLOOD PRESSURE CUFF, REPROCESSED SURGICAL SCISSORS AND GRASPERS, CLEARMEDICAL/HUNTLEIGH FOOT GARMENTS; MODELS FG200/LRG (LARGE), FG200/STD (STANDARD), FG100/SM (SMALL), FG100-R (REGULAR and REPROCESSED TROCARS.

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