FDA applicant

Post Medical, Inc.

Atlanta, GA6 decisions1983–19990 recalls

FDA records 6 decisions for Post Medical, Inc. (Atlanta, GA) from 1983 to 1999: 6 510(k) clearances. Most are in product codes FMI (Needle, Hypodermic, Single Lumen) and KNX (Collector, Urine, (And Accessories) For…). 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 hospital panel, where it files most

How often FDA has decided Post Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Post Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Post”

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

Post Oak Innovations, Inc. 1 Post Operative Pain Management 1

Post Medical, 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?

Other applicant names beginning “Post”