Sharpe Endosurgical Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Sharpe Endosurgical Corp. makes
Sharpe Endosurgical Corp. manufactures the SHARP ENDOKNOT PUSHER and ENDO-ASSIST LAPAROSCOPIC INSTRUMENTS, which are medical devices used in endoscopic and laparoscopic procedures.
The company's devices are classified as Class II and are listed in the FDA 510(k) registry. Sharpe Endosurgical Corp. is based in the US.
Catalogue
Sharp Endoknot Pusher Ref K914967
Regimes: 510(k) Registry: 510(k)Endo-Assist Laparoscopic Instruments Ref K941494
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sharpe Endosurgical Corp. have in the registry?
The registry currently lists 2 devices for Sharpe Endosurgical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sharpe Endosurgical Corp.'s devices?
Among its 2 most recently registered devices, Sharpe Endosurgical Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Sharpe Endosurgical Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Sharpe Endosurgical Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sharpe Endosurgical Corp. in the registry?
The most recently registered devices listed for Sharpe Endosurgical Corp. include SHARP ENDOKNOT PUSHER and ENDO-ASSIST LAPAROSCOPIC INSTRUMENTS.