Poncy, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Poncy, Inc. makes
Poncy, Inc. manufactures single-use medical devices, including needle sticks for procedural use and the Poncy Pak, a disposable packaging system for medical instruments or supplies.
The company’s products are regulated under FDA Class I and Class II classifications, with some devices listed via the 510(k) pathway. Poncy, Inc. is based in the United States.
Catalogue
Needle Stick Ref K885122
Regimes: 510(k) Registry: 510(k)Poncy Pak Ref K791843
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Poncy, Inc. have in the registry?
The registry currently lists 2 devices for Poncy, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Poncy, Inc.'s devices?
Among its 2 most recently registered devices, Poncy, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Poncy, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Poncy, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Poncy, Inc. in the registry?
The most recently registered devices listed for Poncy, Inc. include NEEDLE STICK and PONCY PAK.