Optasia Medical
United KingdomFDA applicant, unverified
- Devices
- 1
What Optasia Medical makes
Optasia Medical produces the SpineAnalyzer Model SAPOC, a device designed for spinal imaging and analysis to assess alignment and curvature in the spine.
The SpineAnalyzer Model SAPOC is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Spineanalyer Model Sapoc Ref K103475
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Optasia Medical have in the registry?
The registry currently lists 1 device for Optasia Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Optasia Medical's devices?
Among its 1 most recently registered device, Optasia Medical has devices listed in FDA 510(k) (1 device).
What risk classes do Optasia Medical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Optasia Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Optasia Medical in the registry?
The most recently registered devices listed for Optasia Medical include SPINEANALYER MODEL SAPOC.