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Porex Medical

Country not established

Devices
15

What Porex Medical makes

Porex Medical manufactures medical implants and surgical instruments, including orbital and malar implants, tissue expanders, nerve locators, and prostheses for facial reconstruction (nose, ear, chin). The company also produces otology instruments, silicone implants for ear, nose, and throat (E.N.T.) procedures, and a bulb drainage system for medical use. Surgical retractors and custom medical implants for orthopedic and reconstructive applications are part of the portfolio.

The company’s devices are classified under FDA categories Class I, Class II, and Unclassified (U), with many authorised via the 510(k) pathway. Products are listed in the FDA’s 510(k) registry. Porex Medical operates from the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does Porex Medical have in the registry?

The registry currently lists 15 devices for Porex Medical. Devices recorded under merged duplicate company entries are counted once.

Which registries list Porex Medical's devices?

Among its 15 most recently registered devices, Porex Medical has devices listed in FDA 510(k) (15 devices).

What risk classes do Porex Medical's devices fall under?

Among its 15 most recently registered devices, the classes recorded for Porex Medical's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Porex Medical in the registry?

The most recently registered devices listed for Porex Medical include POREX(TM) MALAR IMPLANT, POREX(TM) EXTRA-OCULAR ORBITAL IMPLANT, POREX(TM) TISSUE EXPANDER and TLS BULB DRAINAGE SYSTEM.

Generated automatically from registry data and not verified by a human reviewer.