510(k) Report

FDA applicant

Medical Technologies of Georgia

Mchenry, IL13 decisions1978–20080 recalls

FDA records 13 decisions for Medical Technologies of Georgia (Mchenry, IL) from 1978 to 2008: 13 510(k) clearances. Most are in product codes KNX (Collector, Urine, (And Accessories) For…) and KOD (Catheter, Urological). Its devices cite 1 predicate, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Medical Technologies of Georgia, Inc.”.

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

FIG. A — Illustration, gastroenterology and urology panel, where it files most

How often FDA has decided Medical Technologies of Georgia’s devices, and how often a recall has named them.

FDA decisions per year

1in 2008

2008: 1
2007high 1 (2008) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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

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