Promimic AB
SwedenFDA applicant, unverified
- Devices
- 2
What Promimic AB makes
Promimic AB manufactures dental implants with zirconia surfaces, including variants with hydroxyapatite nanocrystal coatings. Their portfolio includes specific implant models with defined diameters (3.75 mm) and lengths (8.5 mm, 10 mm), such as the ZrP Surface and ZrP + HAnano Surface implants.
These devices are classified as Class II under regulatory frameworks and are listed in the FDA’s 510(k) registry. The company is based in Sweden.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Promimic AB have in the registry?
The registry currently lists 2 devices for Promimic AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Promimic AB's devices?
Among its 2 most recently registered devices, Promimic AB has devices listed in FDA 510(k) (2 devices).
What risk classes do Promimic AB's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Promimic AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Promimic AB in the registry?
The most recently registered devices listed for Promimic AB include Promimic ZrP Surface Dental Implant; Promimic ZrP + HAnano Surface Dental Implant and PROMIMIC DENTAL IMPLANT, 3.75 MM, LENGTH 8.5 MM MODEL 03-1001, PROMIMIC DENTAL IMPLANT, 3.75 MM, LENGTH 10 MM MODEL 03-1.