Newclip Technics - FDA 510(k) Cleared Devices

Newclip Technics, is a French manufacturer of orthopedic osteosynthesis solutions based in Haute-Goulaine, near Nantes. The company designs, manufactures, and markets surgical instruments and implants for hospitals and clinics worldwide.

The company has received 31 FDA 510(k) clearances from 31 total submissions since its first clearance in 2006. All submissions focus on orthopedic devices. The latest clearance in 2026 confirms the company remains actively engaged in regulatory submissions and product innovation.

Recent cleared devices include patient-matched instrumentation systems, specialized implants for the hand, wrist, and knee, and plating systems for foot and ankle procedures. The company maintains a global presence across more than 50 countries through nine subsidiaries and an extensive distributor network.

Explore the complete list of Newclip Technics FDA 510(k) cleared devices, including product names, device codes, and clearance dates in the database.

Regulatory submissions have been managed by The OrthoMedix Group, Inc., BioVera, Inc. and The Ortomedix Group, Inc..