Ddc Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
4
Total
4
Cleared
0
Denied
Ddc Technologies, Inc. designs and manufactures aesthetic laser systems for clinical and medical spa applications. Based in Oceanside, the company specializes in cutting-edge laser technology for hair removal, vascular treatments, and pigmentation correction.
The company holds 4 FDA 510(k) clearances from 4 total submissions since 2001. All submissions focus on General & Plastic Surgery devices. The most recent clearance in 2026 confirms active regulatory engagement and ongoing product innovation.
Ddc Technologies' product portfolio includes dual-wavelength Alexandrite/Nd:YAG laser systems and specialized aesthetic laser platforms. The company serves a global network of distributors and clinics with comprehensive training and customer support. Explore the full clearance history, device names, and approval dates in the regulatory database.
FDA 510(k) Regulatory Record - Ddc Technologies, Inc.
4 devices