Superior Biosystems, Inc.
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- Devices
- 1
What Superior Biosystems, Inc. makes
Superior Biosystems, Inc. manufactures the NUPORT PEG Gastrostomy Tube Kit (22 Fr), a medical device designed for percutaneous endoscopic gastrostomy (PEG) procedures to provide long-term enteral nutrition or medication delivery.
The company’s portfolio is regulated under FDA Class II devices, with the NUPORT PEG Gastrostomy Tube Kit authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
No. 87500-Nuport Peg Gastrostomy Tube Kit 22 Fr Ref K894653
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Superior Biosystems, Inc. have in the registry?
The registry currently lists 1 device for Superior Biosystems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Superior Biosystems, Inc.'s devices?
Among its 1 most recently registered device, Superior Biosystems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Superior Biosystems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Superior Biosystems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Superior Biosystems, Inc. in the registry?
The most recently registered devices listed for Superior Biosystems, Inc. include NO. 87500-NUPORT PEG GASTROSTOMY TUBE KIT 22 FR.