Mariner Endosurgery, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Mariner Endosurgery, Inc. makes
Mariner Endosurgery, Inc. manufactures the LaparoGuard, a device designed for laparoscopic procedures to protect abdominal organs during surgery.
The company’s portfolio is regulated under FDA Class II devices, with the LaparoGuard authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
LaparoGuard Ref K182434
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mariner Endosurgery, Inc. have in the registry?
The registry currently lists 1 device for Mariner Endosurgery, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mariner Endosurgery, Inc.'s devices?
Among its 1 most recently registered device, Mariner Endosurgery, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Mariner Endosurgery, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mariner Endosurgery, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mariner Endosurgery, Inc. in the registry?
The most recently registered devices listed for Mariner Endosurgery, Inc. include LaparoGuard.