Endoshape, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Endoshape, Inc. makes
Endoshape, Inc. manufactures the MEDUSA Vascular Plug, a device designed for vascular embolization procedures to occlude blood vessels.
The MEDUSA Vascular Plug is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Medusa Vascular Plug, Ref K140796
Regimes: 510(k) Registry: 510(k)Medusa Vascular Plug Ref K123696
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 788545692
- [email protected]
- Phone
- 844-870-5070
Frequently asked questions
How many devices does Endoshape, Inc. have in the registry?
The registry currently lists 5 devices for Endoshape, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Endoshape, Inc.'s devices?
Among its 5 most recently registered devices, Endoshape, Inc. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Endoshape, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Endoshape, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Endoshape, Inc. in the registry?
The most recently registered devices listed for Endoshape, Inc. include Medusa Multi-Coil MMC074-45, Medusa Multi-Coil MMC-122, Medusa Multi-Coil MMC-120 and MEDUSA VASCULAR PLUG,.