Science Incorporated
United StatesFDA applicant, unverified
- Devices
- 4
What Science Incorporated makes
Science Incorporated manufactures personal infusor devices, including standalone pumps and procedural kits designed for local pain management. Their products incorporate drug disposal septal ports and modular modifications for procedural use, targeting controlled drug administration in clinical settings.
These devices are classified as Class II under FDA regulations and are recorded in the 510(k) premarket notification process. The company is based in the United States.
Catalogue
Personal Infusor With Drug Disposal Septal Port Ref K990208
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Personal Infusor Ref K971362
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Science Incorporated have in the registry?
The registry currently lists 4 devices for Science Incorporated. Devices recorded under merged duplicate company entries are counted once.
Which registries list Science Incorporated's devices?
Among its 4 most recently registered devices, Science Incorporated has devices listed in FDA 510(k) (4 devices).
What risk classes do Science Incorporated's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Science Incorporated's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Science Incorporated in the registry?
The most recently registered devices listed for Science Incorporated include PERSONAL INFUSOR WITH DRUG DISPOSAL SEPTAL PORT, PERSONAL INFUSOR LOCAL PAIN MANAGEMENT PROCEDURAL KIT, PERSONAL INFUSOR and MODIFICATION TO PERSONAL INFUSOR LOCAL PAIN MANAGEMENT PROCEDURAL KIT.