Dr. Jean Bausch GmbH & Co. KG

Dr. Jean Bausch GmbH & Co. KG specializes in dental articulation paper forceps, which are tools used in dentistry to hold and position articulation paper during dental procedures. Their product line includes straight and curved forceps, such as the Arti-Fol®-Forceps with longitudinal grooves or sterile slides, as well as specialized variants like the Arti-Fol® Approximal Contact Forceps and the FIX-CLIP. They also produce Y-shaped holders (e.g., the Bausch Y-Holder) designed to assist with managing dental articulation paper.

Dr. Jean Bausch GmbH & Co. KG has a presence in the United States, though its headquarters or primary location is not specified in the available data. The company’s devices are registered in the FDA’s Unique Device Identifier (UDI) database, indicating compliance with U.S. regulatory requirements for medical devices.

Dr. Jean Bausch GmbH & Co. KG’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is used to track and identify medical devices authorized for commercial distribution in the United States, ensuring traceability and regulatory compliance.

All of Dr. Jean Bausch GmbH & Co. KG’s listed dental articulation paper forceps fall under Class I regulation. This classification applies to low-risk devices that pose minimal potential harm to patients, typically requiring less stringent premarket review by regulatory bodies like the FDA.