The Gillette Company is one of 26010 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Gillette Company - FDA 510(k) Cleared Devices
Recent clearances: DELUXE HEAT WRAP/COLD WRAP, GILLETTE CORDLESS WHIRLPOOL, GILLETTE HEAT WRAP
3
Total
3
Cleared
0
Denied
The Gillette Company, is a men's grooming brand with a manufacturing facility in McHenry, US. The company is known for razors, blade refills, beard trimmers, and personal shaving products.
The company has received 3 FDA 510(k) clearances from 3 total submissions. All cleared devices fall within the Physical Medicine category. The company's regulatory history spans from 1979 to 1980. The company is inactive and represents a historical regulatory record with no recent FDA submissions.
Historical Physical Medicine devices cleared by the company include heat wraps and whirlpool therapy equipment. These products reflect the company's earlier diversification beyond consumer shaving products into therapeutic wellness devices.
Explore the complete list of device names, product codes, and clearance dates in the 510(k) database.
FDA 510(k) Regulatory Record - The Gillette Company
3 devices