Nike, Inc. is one of 9859 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nike, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NIKE V8 AND NIKE V12, MAGNETO EYEWEAR
2
Total
2
Cleared
0
Denied
Nike, Inc. is a global athletic footwear and apparel company with a manufacturing facility in Beaverton, US. The company is primarily known for sportswear and performance footwear across multiple categories.
Nike received 2 FDA 510(k) clearances from 2 total submissions in the Ophthalmic device category. The company's regulatory activity spans from 1996 to 1996. This represents a historical record; Nike has not pursued FDA 510(k) clearances in more than five years and is no longer active in the medical device space.
Historical cleared devices include the NIKE V8 and NIKE V12, as well as MAGNETO EYEWEAR, all within the Ophthalmic category. Explore the full clearance record, including device names, product codes, and clearance dates in the database.
FDA 510(k) Regulatory Record - Nike, Inc.
2 devices