Ongard Meddevice Packaging, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Ongard Meddevice Packaging, Inc. makes
Ongard Meddevice Packaging, Inc. manufactures sterilization pouches and instrument trays designed for medical device packaging, including the AUTOPAK STERILIZATION POUCH and AUTOPAK INSTRUMENT TRAY STERILIZATION POUCH. These products are intended for use in sterilization processes to protect medical instruments and devices during sterilization and storage.
The company’s products fall under FDA Class II medical devices and are listed in the FDA 510(k) registry. The portfolio is regulated under US medical device laws, with compliance required for market distribution in the United States.
Catalogue
Autopak Instrument Tray Sterilization Pouch Ref K932086
Regimes: 510(k) Registry: 510(k)Autopak Sterilization Pouch Ref K932088
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ongard Meddevice Packaging, Inc. have in the registry?
The registry currently lists 2 devices for Ongard Meddevice Packaging, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ongard Meddevice Packaging, Inc.'s devices?
Among its 2 most recently registered devices, Ongard Meddevice Packaging, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Ongard Meddevice Packaging, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ongard Meddevice Packaging, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ongard Meddevice Packaging, Inc. in the registry?
The most recently registered devices listed for Ongard Meddevice Packaging, Inc. include AUTOPAK INSTRUMENT TRAY STERILIZATION POUCH and AUTOPAK STERILIZATION POUCH.