Augerscope, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Augerscope, Inc. makes
Augerscope, Inc. manufactures the CPREVIVER and its modified variant, both of which are endoscopic devices designed for the removal of foreign bodies from the gastrointestinal tract. These tools are intended for use in procedures where retrieval of ingested objects is required, such as in the esophagus or stomach.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance. The devices are listed in the FDA’s 510(k) registry. Augerscope, Inc. is based in the United States.
Catalogue
Modified Cpreviver Ref K871147
510(k) 510(k)Cpreviver Ref K864125
510(k) 510(k)
Frequently asked questions
How many devices does Augerscope, Inc. have in the registry?
The registry currently lists 2 devices for Augerscope, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Augerscope, Inc.'s devices?
Among its 2 most recently registered devices, Augerscope, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Augerscope, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Augerscope, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Augerscope, Inc. in the registry?
The most recently registered devices listed for Augerscope, Inc. include MODIFIED CPREVIVER and CPREVIVER.