Artiness S.r.l.
ItalyFDA applicant, unverified
- Devices
- 1
What Artiness S.r.l. makes
Artiness S.R.L. manufactures the ARTICOR planner, a medical device designed for surgical planning and anatomical mapping, likely used in orthopedic or spinal procedures to assist in preoperative assessments.
The ARTICOR planner is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
ARTICOR planner Ref K252195
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Artiness S.R.L have in the registry?
The registry currently lists 1 device for Artiness S.R.L. Devices recorded under merged duplicate company entries are counted once.
Which registries list Artiness S.R.L's devices?
Among its 1 most recently registered device, Artiness S.R.L has devices listed in FDA 510(k) (1 device).
What risk classes do Artiness S.R.L's devices fall under?
Among its 1 most recently registered device, the classes recorded for Artiness S.R.L's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Artiness S.R.L in the registry?
The most recently registered devices listed for Artiness S.R.L include ARTICOR planner.