Pinyons Medical Technology, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Pinyons Medical Technology, Inc. makes
Pinyons Medical Technology, Inc. manufactures automated medical devices for syringe-based procedures, including the POWRSYRINGE Injector for controlled drug delivery, the POWRSYRINGE Aspirator for fluid extraction, and the POWRSYRINGE Monitor for real-time parameter tracking during procedures.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Powrsyringe Injector Ref K072318
Regimes: 510(k) Registry: 510(k)Powrsyringe Aspirator Ref K072299
Regimes: 510(k) Registry: 510(k)Powrsyringe Monitor Ref K072345
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pinyons Medical Technology, Inc. have in the registry?
The registry currently lists 3 devices for Pinyons Medical Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pinyons Medical Technology, Inc.'s devices?
Among its 3 most recently registered devices, Pinyons Medical Technology, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Pinyons Medical Technology, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Pinyons Medical Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pinyons Medical Technology, Inc. in the registry?
The most recently registered devices listed for Pinyons Medical Technology, Inc. include POWRSYRINGE INJECTOR, POWRSYRINGE ASPIRATOR and POWRSYRINGE MONITOR.