Vesta
Also registered as Vesta, Inc.
Country not established FDA establishment FEI 2182291
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Nasopharyngeal Airway Ref K810960
510(k) 510(k)Silicone Rugger Disposable Yoke-Cpap Ref K834078
510(k) 510(k)Silicone Rubber-Bi Nasopharyngeal Air Ref K792018
510(k) 510(k)3 Way Urethral Irrigation Catheter Ref K792719
510(k) 510(k)
Company details
- FDA FEI number
- 2182291
- Address
- 9900 S 57th St, Franklin, WI, 53132
Frequently asked questions
How many devices does VESTA have in the registry?
The registry currently lists 4 devices for VESTA. Devices recorded under merged duplicate company entries are counted once.
Which registries list VESTA's devices?
Among its 4 most recently registered devices, VESTA has devices listed in FDA 510(k) (4 devices).
What risk classes do VESTA's devices fall under?
Among its 4 most recently registered devices, the classes recorded for VESTA's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from VESTA in the registry?
The most recently registered devices listed for VESTA include NASOPHARYNGEAL AIRWAY, SILICONE RUGGER DISPOSABLE YOKE-CPAP, SILICONE RUBBER-BI NASOPHARYNGEAL AIR and 3 WAY URETHRAL IRRIGATION CATHETER.