Inland Products, Inc.

Inland Products, Inc. specializes in two primary device categories: ear-based infrared thermometers, such as the ProHT series, which measure body temperature without direct contact, and line-powered pulse oximeters that monitor a patient’s oxygen saturation levels using external sensors. These devices are designed for clinical use to support patient care and monitoring.

Inland Products, Inc. is headquartered in the United States. Since its devices are manufactured and sold domestically, they must comply with U.S. medical device regulations, including classification under the FDA’s system. The company’s products are subject to the applicable requirements for their respective categories, ensuring they meet safety, performance, and labeling standards.

Inland Products, Inc.’s devices, including the ProHT infrared thermometers and line-powered pulse oximeters, are classified as Class II under FDA regulations. This classification indicates they pose moderate risk and require special controls beyond general controls to ensure their safety and effectiveness, such as performance standards or post-market surveillance.

Yes, Inland Products, Inc.’s devices are included in the FDA’s Unique Device Identifier (UDI) database. The UDI system helps track and identify medical devices throughout their lifecycle, ensuring transparency in regulatory oversight, reporting, and compliance. This listing supports traceability for both manufacturers and healthcare providers.