510(k) Report

FDA applicant

Fertility Technology Resources, Inc.

Marietta, GA4 decisions1999–20042 recalls

FDA records 4 decisions for Fertility Technology Resources, Inc. (Marietta, GA) from 1999 to 2004: 4 510(k) clearances. Most are in product codes MQF (Catheter, Assisted Reproduction) and MQE (Needle, Assisted Reproduction). 2 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Fertility Technology Resources, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Fertility Technology Resources, Inc. since 2007.

Recalls per year

2in 2007

2007: 2
2007high 2 (2007) · low 0 (2008)2026

Class I Class II/III not classified

FIG. 1 — Fertility Technology Resources, 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 “Fertility”

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