Endo-Scientific, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Endo-Scientific, Inc. makes
Endo-Scientific, Inc. manufactures disposable biopsy forceps designed for use with flexible endoscopes, as well as the Guardian forceps, a reusable device for tissue sampling and retrieval during endoscopic procedures.
The company’s products are regulated under FDA’s 510(k) pathway, with devices classified as Class I and Class II. They are listed in the FDA’s 510(k) clearance registry, and the manufacturer is based in the United States.
Catalogue
Disposable Biopsy Forcep For Flexible Endoscopes Ref K902066
Regimes: 510(k) Registry: 510(k)Guardian Forcep Ref K893636
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Endo-Scientific, Inc. have in the registry?
The registry currently lists 2 devices for Endo-Scientific, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Endo-Scientific, Inc.'s devices?
Among its 2 most recently registered devices, Endo-Scientific, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Endo-Scientific, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Endo-Scientific, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Endo-Scientific, Inc. in the registry?
The most recently registered devices listed for Endo-Scientific, Inc. include DISPOSABLE BIOPSY FORCEP FOR FLEXIBLE ENDOSCOPES and GUARDIAN FORCEP.