Km Corp.
Country not established
- Devices
- 4
What Km Corp. makes
Km Corp. manufactures the Perpak Sterilization Tyvek Pouch, a barrier pouch designed for medical device sterilization and protection during storage and transport.
The company’s portfolio is regulated under FDA’s Class II device classification and is listed via the 510(k) pathway. The product is based in the United States.
Catalogue
Enaden Flow Ref K140976
Regimes: 510(k) Registry: 510(k)Trc-Paste Ref K133716
Regimes: 510(k) Registry: 510(k)Trc-Pex, Radic-Sealer Ref K132123
Regimes: 510(k) Registry: 510(k)Perpak™ Sterilization Tyvek Pouch Ref K241123
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Km Corp. have in the registry?
The registry currently lists 4 devices for Km Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Km Corp.'s devices?
Among its 4 most recently registered devices, Km Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do Km Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Km Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Km Corp. in the registry?
The most recently registered devices listed for Km Corp. include ENADEN FLOW, TRC-PASTE, TRC-PEX, RADIC-SEALER and Perpak™ Sterilization Tyvek Pouch.