Depuyacromed
Country not established
- Devices
- 49
What Depuyacromed makes
The company manufactures spinal fixation and fusion systems, including titanium spinal rods, cage systems for interbody fusion, and connectors for rod stabilization. Their portfolio includes the Isola Spinal System with dual-rod connectors, the Symphony Graft Delivery System for bone graft placement, and the MOSS Miami Spine System with pedicle and laminar hooks. Additional products cover cranial fixation, such as the Bremer Halo System titanium skull pins, and modular components for spinal surgery like the VBR and Crossover Connectors.
These devices are regulated under FDA classifications, including Class I, Class II, and Unclassified (U), with most submissions supported by 510(k) clearances. The portfolio is listed in the FDA’s 510(k) registry, reflecting their authorised spinal and cranial fixation solutions. The company is based in the United States.
Catalogue
Search and filter all 49 devicesFrequently asked questions
How many devices does Depuyacromed have in the registry?
The registry currently lists 49 devices for Depuyacromed. Devices recorded under merged duplicate company entries are counted once.
Which registries list Depuyacromed's devices?
Among its 49 most recently registered devices, Depuyacromed has devices listed in FDA 510(k) (49 devices).
What risk classes do Depuyacromed's devices fall under?
Among its 49 most recently registered devices, the classes recorded for Depuyacromed's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Depuyacromed in the registry?
The most recently registered devices listed for Depuyacromed include MOSS MIAMI SPINAL SYSTEMS, MONARCH SPINE SYSTEM, EAGLE ANTERIOR CERVIAL PLATE SYSTEM and STACKABLE CAGE SYSTEM.