AJL OPHTHALMIC SA

AJL OPHTHALMIC SA makes oropharyngeal airways, which are single-use medical devices designed to maintain a patient's airway. An example of their product is the VAMA. The company's portfolio consists of these airway management devices, which are used in clinical settings to support breathing during procedures or emergencies.

AJL OPHTHALMIC SA is based in the United States, as indicated by the country field in the device data. The company operates from this location, and its devices are subject to regulatory oversight in the US market where they are manufactured and distributed.

AJL OPHTHALMIC SA's devices are listed in the FDA UDI registry. This registry contains information about medical devices marketed in the United States, including device identifiers and other regulatory details. The listing confirms that the company's products are part of the U.S. medical device tracking system.

AJL OPHTHALMIC SA's devices are classified as Class I medical devices. This classification indicates they are subject to the lowest level of regulatory control, typically because they pose low risk to patients. Class I devices are generally subject to general controls such as labeling and manufacturing practices, but not premarket approval.