Medicon EG
Country not established FDA
- Devices
- 17
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Medicon EG makes
Medicon EG manufactures mandibular reconstruction plating systems, sternal closure systems, cranio maxillofacial titanium implant systems, titanium miniplate systems, anchorage systems, mandibular distraction devices, micro titanium plate systems, and surgical instruments such as clip applying forceps and headrest clamp systems.
The devices are classified as Class II and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Search and filter all 17 devicesFDA establishments
- Medicon, E.G. TUTTLINGEN Baden-Wurttemberg · DE Other ID 5870
Frequently asked questions
How many devices does Medicon EG have in the registry?
The registry currently lists 17 devices for Medicon EG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medicon EG's devices?
Among its 17 most recently registered devices, Medicon EG has devices listed in FDA 510(k) (17 devices).
What risk classes do Medicon EG's devices fall under?
Among its 17 most recently registered devices, the classes recorded for Medicon EG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medicon EG in the registry?
The most recently registered devices listed for Medicon EG include MEDICON 2.4 MANDIBULAR RECONSTRUCTION PLATING SYSTEM, MEDICON STERN-A-FIX STERNAL CLOSURE SYSTEM, CMS CRANIO MAXILLO FACIAL TITANIUM IMPLANT SYSTEM and TITANIUM MINIPLATE SYSTEM.
Which FDA establishments are linked to Medicon EG?
1 FDA establishment is linked to Medicon EG in the registry; they are listed on the company page.