Porex Technologies Corp. of Georgia
United StatesFDA applicant, unverified
- Devices
- 2
What Porex Technologies Corp. of Georgia makes
Porex Technologies Corp. of Georgia manufactures ossicular prostheses, including both partial and total replacements for middle ear bone structures, as well as the MEDPOR Ocular PEG System and its associated accessories.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Ossicular Prosthesis: 8 Partial, 3 Total Ref K884884
Regimes: 510(k) Registry: 510(k)Medpor Ocular Peg System And Accessories Ref K960859
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Porex Technologies Corp. of Georgia have in the registry?
The registry currently lists 2 devices for Porex Technologies Corp. of Georgia. Devices recorded under merged duplicate company entries are counted once.
Which registries list Porex Technologies Corp. of Georgia's devices?
Among its 2 most recently registered devices, Porex Technologies Corp. of Georgia has devices listed in FDA 510(k) (2 devices).
What risk classes do Porex Technologies Corp. of Georgia's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Porex Technologies Corp. of Georgia's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Porex Technologies Corp. of Georgia in the registry?
The most recently registered devices listed for Porex Technologies Corp. of Georgia include OSSICULAR PROSTHESIS: 8 PARTIAL, 3 TOTAL and MEDPOR OCULAR PEG SYSTEM AND ACCESSORIES.