Lanterna Medical Technologies
Country not established
- Devices
- 268
What Lanterna Medical Technologies makes
Lanterna Medical Technologies manufactures internal spinal fixation systems, including pre-bent and straight rods, cannulated and non-cannulated polyaxial pedicle screws, and reduction polyaxial pedicle screws. These devices are designed for bone fixation in spinal procedures, available in both sterile and non-sterile configurations. Product sizes vary by diameter and length to accommodate different surgical needs.
The company’s portfolio is regulated under FDA Class II devices and is listed in the FDA’s 510(k) and Unique Device Identification (UDI) registries. The manufacturer is based in the United States.
Catalogue
Search and filter all 268 devicesShowing 1-50 of 268
Frequently asked questions
How many devices does Lanterna Medical Technologies have in the registry?
The registry currently lists 268 devices for Lanterna Medical Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lanterna Medical Technologies's devices?
Among its 50 most recently registered devices, Lanterna Medical Technologies has devices listed in FDA GUDID (50 devices).
What risk classes do Lanterna Medical Technologies's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Lanterna Medical Technologies's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lanterna Medical Technologies in the registry?
The most recently registered devices listed for Lanterna Medical Technologies include Santis Pre Bent Rod 5.5mmx180mm 101-0180, Santis Cannulated Polyaxial Pedicle Screw/Dia.5.5mm/Lng.30mm 501-5530, Santis Cannulated Reduction Polyaxial Pedicle Screw/Dia.5.5mm/Lng.35mm 701-5535 and Santis Non Cannulated Reduction Polyaxial Pedicle Screw/Dia.6.5mm/Lng.50mm 801-6550.