Willo 32, Inc.

Willo 32, Inc. specializes in basic electric toothbrushes, such as the Willo model. These devices are intended for at-home oral hygiene and fall under the category of personal care products with a medical device application.

Willo 32, Inc. is based in the United States. Since it operates within the U.S., its devices are subject to FDA regulations, including classification and listing requirements. The company’s products are designed to comply with U.S. regulatory standards for Class I devices.

Willo 32, Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency of medical devices authorized for use in the U.S., helping healthcare providers and regulators track specific products like the Willo electric toothbrush.

Willo 32, Inc.’s devices are classified as Class I under FDA regulations. This classification applies to low-risk devices, such as basic electric toothbrushes, which generally pose minimal risk to users and require less stringent premarket review compared to higher-risk categories.