FDA applicant

Porex Surgical Products Group

Newnan, GA1 decision2000–20000 recalls

FDA records 1 decision for Porex Surgical Products Group (Newnan, GA) in 2000: 1 510(k) clearance. All are in product code MNF (Implant, Temporal). 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, general and plastic surgery panel, where it files most

How often FDA has decided Porex Surgical Products Group’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Porex Surgical Products Group since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Porex Surgical Products Group 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 Technologies Corp. of Georgia 2 Porex Medical Products 1

Porex Surgical Products Group

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”