Prosper, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Prosper, Inc. makes
Prosper, Inc. manufactures the STAPLE REMOVER SR300P, a handheld device for safely removing surgical staples, and the SKIN STAPLING DEVICE SC2000, used for closing small skin incisions with staples.
These products are classified as Class I medical devices and are listed under FDA 510(k) clearance. The company is based in the United States.
Catalogue
Staple Remover SR300P Ref K833085
Regimes: 510(k) Registry: 510(k)Skin Stapling Device SC2000 Ref K832709
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Prosper, Inc. have in the registry?
The registry currently lists 2 devices for Prosper, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Prosper, Inc.'s devices?
Among its 2 most recently registered devices, Prosper, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Prosper, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Prosper, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Prosper, Inc. in the registry?
The most recently registered devices listed for Prosper, Inc. include STAPLE REMOVER SR300P and SKIN STAPLING DEVICE SC2000.