FDA applicant

Porex Technologies Corp. of Georgia

Fairburn, GA2 decisions1989–19960 recalls

FDA records 2 decisions for Porex Technologies Corp. of Georgia (Fairburn, GA) from 1989 to 1996: 2 510(k) clearances. Most are in product codes HPZ (Implant, Eye Sphere) and ETA (Replacement, Ossicular Prosthesis, Total). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, ophthalmic panel, where it files most

How often FDA has decided Porex Technologies Corp. of Georgia’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Porex Technologies Corp. of Georgia since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Porex Technologies Corp. of Georgia by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Porex”

FDA records each applicant name separately; these may or may not be the same firm.

Porex Surgical, Inc. 19 Porex Medical 15 Porex Technologies Corp. 2 Porex Medical Products 1 Porex Surgical Products Group 1

Porex Technologies Corp. of Georgia

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Porex”