FIBEROPTIC BULBS, INC.

Fiberoptic Bulbs, Inc. specializes in head-worn lamps for medical use, such as the FOBI Medical device. These products are designed to provide focused illumination during clinical procedures or examinations, ensuring better visibility for healthcare professionals.

The company is headquartered in the United States, where it develops and manufactures its medical illumination devices.

Yes, the company’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S., ensuring traceability and compliance.

Fiberoptic Bulbs, Inc.’s products fall under the FDA’s Class I medical device classification. This category generally includes low-risk devices that pose minimal potential harm to patients, often requiring less stringent regulatory oversight.