Corptomic
Country not established
- Devices
- 1
What Corptomic makes
Corptomic manufactures the CORATOMIC Model Ovalith-920BP, a Class III medical device designed for cardiac ablation procedures, intended to treat arrhythmias by creating precise lesions in heart tissue.
The Ovalith-920BP is regulated under the FDA’s 510(k) pathway as a Class III device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Coratomic Model Ovalith-920BP Ref K811768
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Corptomic have in the registry?
The registry currently lists 1 device for Corptomic. Devices recorded under merged duplicate company entries are counted once.
Which registries list Corptomic's devices?
Among its 1 most recently registered device, Corptomic has devices listed in FDA 510(k) (1 device).
What risk classes do Corptomic's devices fall under?
Among its 1 most recently registered device, the classes recorded for Corptomic's devices are Class III. Each device page shows its own class and authorisation.
What are the newest devices from Corptomic in the registry?
The most recently registered devices listed for Corptomic include CORATOMIC MODEL OVALITH-920BP.