Boston Endo-Surgical Technologies, Inc.
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- Devices
- 1
What Boston Endo-Surgical Technologies, Inc. makes
Boston Endo-Surgical Technologies, Inc. manufactures bipolar forceps, a type of electrosurgical instrument used in minimally invasive procedures to cut and coagulate tissue simultaneously during endoscopic surgeries.
The company’s bipolar forceps are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Bipolar Forceps Ref K131058
510(k) 510(k)
Frequently asked questions
How many devices does Boston Endo-Surgical Technologies, Inc. have in the registry?
The registry currently lists 1 device for Boston Endo-Surgical Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Boston Endo-Surgical Technologies, Inc.'s devices?
Among its 1 most recently registered device, Boston Endo-Surgical Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Boston Endo-Surgical Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Boston Endo-Surgical Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Boston Endo-Surgical Technologies, Inc. in the registry?
The most recently registered devices listed for Boston Endo-Surgical Technologies, Inc. include BIPOLAR FORCEPS.