VIVID MEDICAL INC.

Vivid Medical Inc. specializes in channeled video intubation laryngoscopes, which are used to assist medical professionals during airway management procedures. These devices combine video technology with traditional laryngoscope design to provide real-time visual feedback, enhancing precision and visibility during intubation. The focus is on improving procedural safety and efficiency in critical care settings.

Vivid Medical Inc. is headquartered in the United States, which means its devices are subject to FDA regulatory requirements. Since the company’s products fall under Class I classification, they are generally considered low-risk, but they still must comply with FDA registration and UDI (Unique Device Identifier) listing requirements to ensure traceability and market transparency.

Yes, Vivid Medical Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is critical because it ensures transparency in the medical device supply chain, allowing healthcare providers, regulators, and manufacturers to track devices throughout their lifecycle. Listing in the UDI database also helps verify compliance with FDA requirements for device identification and reporting.

Vivid Medical Inc.’s devices are classified as Class I by regulatory authorities. This classification typically applies to low-risk medical devices, such as some surgical instruments or patient monitoring equipment. While Class I devices generally require less stringent premarket review, they still must meet basic safety and performance standards, and manufacturers must adhere to FDA registration and UDI requirements to ensure compliance and market access.