Porex Technologies Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Porex Technologies Corp. makes
Porex Technologies Corp. manufactures porous polyethylene implants and accessories for cranial and facial reconstruction, including the MEDPOR Ocular Screw and preformed cranial/facial implants designed for surgical applications.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Medpor Ocular Screw And Acceossories Ref K971583
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Porex Technologies Corp. have in the registry?
The registry currently lists 2 devices for Porex Technologies Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Porex Technologies Corp.'s devices?
Among its 2 most recently registered devices, Porex Technologies Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Porex Technologies Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Porex Technologies Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Porex Technologies Corp. in the registry?
The most recently registered devices listed for Porex Technologies Corp. include MEDPOR OCULAR SCREW AND ACCEOSSORIES and MEDPOR SURG IMPLANT MATERIAL:PREFOR CRAN/FAC IMPLA.