Southside Biotechnology
Country not established
- Devices
- 3
What Southside Biotechnology makes
Southside Biotechnology manufactures gastrostomy feeding devices, including percutaneous endoscopic gastrostomy (PEG) feeding catheters and related tubing for nutritional support in patients requiring long-term enteral feeding.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States.
Catalogue
Gastrostomy Feeding Device Ref K884439
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Gastrostomy Feeding Catheter Ref K901795
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Southside Biotechnology have in the registry?
The registry currently lists 3 devices for Southside Biotechnology. Devices recorded under merged duplicate company entries are counted once.
Which registries list Southside Biotechnology's devices?
Among its 3 most recently registered devices, Southside Biotechnology has devices listed in FDA 510(k) (3 devices).
What risk classes do Southside Biotechnology's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Southside Biotechnology's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Southside Biotechnology in the registry?
The most recently registered devices listed for Southside Biotechnology include GASTROSTOMY FEEDING DEVICE, PERCUTANEOUS ENDOSCOPIC GASTROSTOMY FEEDING CATH. and GASTROSTOMY FEEDING CATHETER.