Portec, Inc.
Country not established
- Devices
- 1
What Portec, Inc. makes
Portec, Inc. manufactures the PORT-OP, a device designed for postoperative drainage in surgical procedures, helping manage fluid accumulation after operations.
The PORT-OP is classified as a Class I medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Port-Op Ref K813106
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Portec, Inc. have in the registry?
The registry currently lists 1 device for Portec, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Portec, Inc.'s devices?
Among its 1 most recently registered device, Portec, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Portec, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Portec, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Portec, Inc. in the registry?
The most recently registered devices listed for Portec, Inc. include PORT-OP.