Alcon Laboratories is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alcon Laboratories - FDA 510(k) Cleared Devices
Alcon Laboratories, is a Swiss-American pharmaceutical and medical device company specializing in eye care products. The company maintains operational headquarters in Fort Worth, Texas, with a significant global presence in eye care innovation.
Alcon has received 47 FDA 510(k) clearances from 47 total submissions since its first clearance in 1976. The company's regulatory portfolio is dominated by Ophthalmic devices, which account for 74% of all submissions. The latest clearance on record dates to 2007, reflecting the company's historical significance in the medical device regulatory landscape.
Alcon's cleared device portfolio encompasses a broad range of Ophthalmic technologies. These include intraocular lens delivery systems, contact lens care solutions, laser surgical systems, and enzymatic cleaning products. The company's product portfolio reflects deep expertise in vision correction and ocular surgical support.
Explore the complete regulatory history of Alcon Laboratories by reviewing individual device names, product codes, and clearance dates in the database.
FDA 510(k) Regulatory Record - Alcon Laboratories
Looking for a specific device from Alcon Laboratories? Search by device name or K-number.
Search all Alcon Laboratories devices