Tautona Group Research & Development, Co., LLC
Country not established
- Devices
- 1
What Tautona Group Research & Development, Co., LLC makes
Tautona Group Research & Development, Co., LLC manufactures the TauTona Pneumoperitoneum Assist Device (TPAD), a medical device designed to assist in creating pneumoperitoneum during laparoscopic procedures.
The TPAD is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
TauTona Pneumoperitoneum Assist Device (TPAD) Ref K233020
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tautona Group Research & Development, Co., LLC have in the registry?
The registry currently lists 1 device for Tautona Group Research & Development, Co., LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tautona Group Research & Development, Co., LLC's devices?
Among its 1 most recently registered device, Tautona Group Research & Development, Co., LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Tautona Group Research & Development, Co., LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Tautona Group Research & Development, Co., LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tautona Group Research & Development, Co., LLC in the registry?
The most recently registered devices listed for Tautona Group Research & Development, Co., LLC include TauTona Pneumoperitoneum Assist Device (TPAD).