Taylor H. Haynes, M.D.
Country not established
- Devices
- 1
What Taylor H. Haynes, M.D. makes
Taylor H. Haynes, M.D. manufactures the Power Suture, a device designed for tissue approximation and wound closure in surgical procedures.
The Power Suture is classified under FDA’s 510(k) pathway, indicating it is regulated as a Class II medical device in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Power Suture Ref K821702
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Taylor H. Haynes, M.D. have in the registry?
The registry currently lists 1 device for Taylor H. Haynes, M.D.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Taylor H. Haynes, M.D.'s devices?
Among its 1 most recently registered device, Taylor H. Haynes, M.D. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Taylor H. Haynes, M.D. in the registry?
The most recently registered devices listed for Taylor H. Haynes, M.D. include POWER SUTURE.