curasan AG
Country not established
curasan AG is a medical device manufacturer, with 167 devices listed in 4 registries (FDA Class II; EU Class III, I and IIb) as of 13 Nov 2026.
- Devices
- 167
Registry facts
- Registries
- FDA GUDID 100
- EUDAMED 70
- FDA 510(k) 10
- FDA PMA 1
- Device classes
- FDA Class II 103
- EU Class III 49
- EU Class I 4
- EU Class IIb 4
- Top EMDN categories
- Sites and related companies
- Curasan AG Germany
- Identifiers
- DUNS 324331826
What curasan AG makes
curasan AG manufactures synthetic and composite bone matrix implants for dental and orthopedic applications, including hydroxyapatite-based grafts, beta-tricalcium phosphate (β-TCP) particles, and resorbable ceramic materials for bone regeneration.
These products are classified as Class II medical devices and are authorised via FDA pathways including 510(k), PMA, and UDI registrations.
Catalogue
Search and filter all 167 devicesShowing 1-50 of 167
Company details
- DUNS number
- 324331826
- info@curasan.de
- Phone
- +496027409000
Sites
- Curasan AG DEFEI 3003771570 57 devices
Frequently asked questions
How many devices does curasan AG have in the registry?
The registry currently lists 167 devices for curasan AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list curasan AG's devices?
Among its 50 most recently registered devices, curasan AG has devices listed in EUDAMED (33 devices) and FDA GUDID (17 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do curasan AG's devices fall under?
Among its 50 most recently registered devices, the classes recorded for curasan AG's devices are Class I, Class IIb, Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from curasan AG in the registry?
The most recently registered devices listed for curasan AG include CERACELL®, Ti-System® Titanium Pins, Ti-SYSTEM Screwdriver and CERASORB® Bioactive.