Telltale, LLC
Country not established
- Devices
- 1
What Telltale, LLC makes
Telltale, LLC manufactures the Telltale Electrosurgical Guidewire System, a device designed to assist in the precise placement of guidewires during electrosurgical procedures, improving navigation and safety in minimally invasive surgeries.
The Electrosurgical Guidewire System is classified as a Class II medical device in the US and is authorised through the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
TELLTALE Electrosurgical Guidewire System Ref K252592
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Telltale, LLC have in the registry?
The registry currently lists 1 device for Telltale, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Telltale, LLC's devices?
Among its 1 most recently registered device, Telltale, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Telltale, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Telltale, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Telltale, LLC in the registry?
The most recently registered devices listed for Telltale, LLC include TELLTALE Electrosurgical Guidewire System.