Synthes
Country not established
Part of Synthes GmbH
Synthes is a medical device manufacturer, with 617 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (FDA Class II and I) as of 13 Nov 2026.
- Devices
- 617
Registry facts
- Registries
- FDA GUDID 598
- EUDAMED 32
- FDA 510(k) 19
- Device classes
- FDA Class II 536
- FDA Class I 81
- Sites and related companies
What Synthes makes
The company manufactures orthopaedic fixation hardware, including non-bioabsorbable plates and screws for bone stabilization, as well as spinal implants such as trial devices, interbody fusion cages, and spinal screws and plates. It also produces craniofacial fixation plates for non-customized facial reconstruction and surgical instrument racks for organizing implants and tools. The portfolio includes specific devices like RapidSorb, MatrixMIDFACE, MatrixMANDIBLE, and various models of the DHS and LCP systems.
These devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States, adhering to applicable U.S. regulatory requirements for medical devices.
Catalogue
Search and filter all 617 devicesShowing 1-50 of 617
Frequently asked questions
How many devices does Synthes have in the registry?
The registry currently lists 617 devices for Synthes. Devices recorded under merged duplicate company entries are counted once.
Which registries list Synthes's devices?
Among its 50 most recently registered devices, Synthes has devices listed in FDA GUDID (50 devices).
What risk classes do Synthes's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Synthes's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Synthes in the registry?
The most recently registered devices listed for Synthes include KINCISE 200002205, TriLEAP 04.900.079, TriLEAP 04.900.080 and TriLEAP 04.900.081.