Upstream Peripheral Technologies
Country not established FDA
- Devices
- 9
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
Catalogue
- GUDID
- GUDID
- GUDID
- GUDID
GoBack Crossing Catheter Ref K211802
510(k) 510(k)- 510(k) 510(k)
Upstream Support Catheter Ref K112886
510(k) 510(k)Upstream GoBack Crossing Catheter Ref K182937
510(k) 510(k)Upstream Gr Catheter Ref K120964
510(k) 510(k)
FDA establishments
- Upstream Peripheral Technologies Ltd. Caesarea Central · IL FEI 3009561706
Frequently asked questions
How many devices does Upstream Peripheral Technologies have in the registry?
The registry currently lists 9 devices for Upstream Peripheral Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Upstream Peripheral Technologies's devices?
Among its 9 most recently registered devices, Upstream Peripheral Technologies has devices listed in FDA 510(k) (5 devices) and FDA GUDID (4 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Upstream Peripheral Technologies's devices fall under?
Among its 9 most recently registered devices, the classes recorded for Upstream Peripheral Technologies's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Upstream Peripheral Technologies in the registry?
The most recently registered devices listed for Upstream Peripheral Technologies include GoBack Crossing Catheter GB 600-US 018P 80L, GoBack Crossing Catheter GB 603-US 014P 80L, GoBack Crossing Catheter GB 603-US 014P 120L and GoBack Crossing Catheter GB 600-US 018P 120L.
Which FDA establishments are linked to Upstream Peripheral Technologies?
1 FDA establishment is linked to Upstream Peripheral Technologies in the registry; they are listed on the company page.