Vibrynt, Inc.
Country not established
- Devices
- 1
What Vibrynt, Inc. makes
Vibrynt, Inc. manufactures flexible endoscopes and guidewires for diagnostic and procedural use in gastrointestinal procedures. The portfolio includes 89 cm and 56 cm endoscopes, as well as blunt-tipped guidewires in lengths of 106 cm, 86 cm, and 53 cm, designed for navigation and visualization within the digestive tract.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vibrynt, Inc. have in the registry?
The registry currently lists 1 device for Vibrynt, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vibrynt, Inc.'s devices?
Among its 1 most recently registered device, Vibrynt, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Vibrynt, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Vibrynt, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vibrynt, Inc. in the registry?
The most recently registered devices listed for Vibrynt, Inc. include VISTA ENDOSCOPE, 89 CM, 56CM, SCOUT BLUNT-TIPPED GUIDE- 106 CM, 86 CM, 53 CM, MODELS FG0027, FG0031, FG0029, FG 0028,.