510(k) Report

FDA applicant

Georgia Biomedical Research Group, Inc.

Macon, GA1 decision1993–19930 recalls

FDA records 1 decision for Georgia Biomedical Research Group, Inc. (Macon, GA) in 1993: 1 510(k) clearance. All are in product code HIF (Insufflator, Laparoscopic). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Georgia Biomedical Research Group, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Georgia Biomedical Research Group, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • HIFInsufflator, Laparoscopic1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K920205Ott Insufflation Filter TubingGeorgia Biomedical Research Group, Inc. · 19931cites it

What has FDA decided for it lately?

  • K920205Ott Insufflation Filter TubingGeorgia Biomedical Research Group, Inc. · 1993

The one decision as Georgia Biomedical Research Group, Inc. →

Other applicant names beginning “Georgia”

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

Georgia Biomedical, Inc. 1Georgia Medical Products, Inc. 1