Peytant Solutions, Inc.
Country not established
- Devices
- 2
What Peytant Solutions, Inc. makes
Peytant Solutions, Inc. manufactures the AMStent® Tracheobronchial Covered Stent System, a device designed for the placement within the tracheobronchial tree to maintain airway patency in patients with obstructions or strictures.
The AMStent® Tracheobronchial Covered Stent System is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- Registry: GUDID
AMStent® Tracheobronchial Covered Stent System Ref DEN230087
Regimes: De Novo Registry: De Novo
Company details
- DUNS number
- 808218015
- [email protected]
- Phone
- 7634508802
Frequently asked questions
How many devices does Peytant Solutions, Inc. have in the registry?
The registry currently lists 2 devices for Peytant Solutions, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Peytant Solutions, Inc.'s devices?
Among its 2 most recently registered devices, Peytant Solutions, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Peytant Solutions, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Peytant Solutions, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Peytant Solutions, Inc. in the registry?
The most recently registered devices listed for Peytant Solutions, Inc. include AMstent Tracheobronchial Covered Stent System AMS1040 and AMStent® Tracheobronchial Covered Stent System.