FDA applicant

Porex Technologies Corp.

Fairburn, GA2 decisions1992–19971 recall

FDA records 2 decisions for Porex Technologies Corp. (Fairburn, GA) from 1992 to 1997: 2 510(k) clearances. Most are in product codes MQU (Ocular Peg) and FWP (Prosthesis, Chin, Internal). 1 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.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Porex Technologies Corp. since 2007.

Recalls per year

1in 2014

2007high 1 (2014) · low 0 (2007)2026

Class I Class II/III not classified

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

Planning a device like Porex Technologies Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

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. of Georgia 2 Porex Medical Products 1 Porex Surgical Products Group 1

Porex Technologies Corp.

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?

What has been recalled?

Other applicant names beginning “Porex”