FDA applicant

Microbio-Medics, Inc.

Columbus, MS13 decisions1988–19938 recalls

FDA records 13 decisions for Microbio-Medics, Inc. (Columbus, MS) from 1988 to 1993: 13 510(k) clearances. Most are in product codes ETA (Replacement, Ossicular Prosthesis, Total) and EPP (Splint, Nasal). 8 recalls are linked to its devices.

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

FIG. A — Illustration, ear, nose and throat panel, where it files most

How often FDA has decided Microbio-Medics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Microbio-Medics, Inc. since 2007.

Recalls per year

1in 2016

2007high 7 (2013) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Microbio-Medics, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Microbio-Medics, Inc.

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?