Dermalogica, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dermalogica, LLC - FDA 510(k) Cleared Devices
Recent clearances: PRO Pen Microneedling System (6883)
1
Total
1
Cleared
0
Denied
Dermalogica, LLC is a professional-grade skin care company with a manufacturing facility in Carson, US. The brand specializes in dermatological skin care products and has expanded into medical device innovation.
The company has received 1 FDA 510(k) clearance from 1 total submission. Dermalogica's cleared device falls within the General & Plastic Surgery category. The company achieved its first FDA 510(k) clearance in 2025 and remains active in the medical device space.
Dermalogica's FDA-cleared device portfolio includes advanced treatment systems designed for professional aesthetic and surgical applications. The company continues to develop innovative solutions that bridge professional skin care expertise with medical device technology.
Explore the company's cleared device names, product codes, and clearance dates in the database above.
FDA 510(k) Regulatory Record - Dermalogica, LLC
1 devices