PIERREL SPA

Pierrel SPA specializes in oral lesion examination lights, such as the G.o.c.c.l.e.s. light. These devices are specifically designed for clinicians to visually inspect oral tissues during medical examinations, improving diagnostic accuracy in oral health assessments.

Pierrel SPA operates from the United States, serving as the headquarters and primary location for its medical device manufacturing and distribution.

Pierrel SPA’s devices, including the G.o.c.c.l.e.s. light, fall under Class II classification. This classification is determined by regulatory authorities based on factors like the device’s intended use, potential risks, and the level of oversight required to ensure safety and effectiveness.

Yes, Pierrel SPA’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices in the U.S. market, ensuring transparency and traceability for healthcare providers and regulators.