Bypass, Ltd.
Country not established
- Devices
- 2
What Bypass, Ltd. makes
Bypass, Ltd. manufactures automated anastomotic devices designed for vascular suturing, including models for vessels ranging from 2.0 to 6.0 mm in outer diameter. These devices facilitate precise surgical connections in blood vessels, reducing manual stitching time and improving procedural efficiency.
The company’s products fall under FDA Class II medical devices and are authorised via the 510(k) clearance pathway. The portfolio is listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
- 510(k) 510(k)
- 510(k) 510(k)
Frequently asked questions
How many devices does Bypass, Ltd. have in the registry?
The registry currently lists 2 devices for Bypass, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bypass, Ltd.'s devices?
Among its 2 most recently registered devices, Bypass, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Bypass, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Bypass, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bypass, Ltd. in the registry?
The most recently registered devices listed for Bypass, Ltd. include MODIFICATION TO CORLINK AUTOMATED ANASTOMOTIC DEVICE and CORLINK AAD (3.5 TO 6.0 M M OUTER DIAMETER VESSELS), MODEL 200-064, CORLINK AAD (2.0 TO 4.0 MM OUTER DIAMETER VESSELS), M.