510(k) Report

FDA applicant

Life Global Group, LLC

Gilford, CT3 decisions2015–20162 recalls

FDA records 3 decisions for Life Global Group, LLC (Gilford, CT) from 2015 to 2016: 3 510(k) clearances. Most are in product codes MQL (Media, Reproductive) and MQH (Microtools, Assisted Reproduction (Pipettes)). 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 Life Global Group, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2015: 22016: 1
2015high 2 (2015) · low 0 (2017)2026

2026 so far, outlined.

Recalls per year

2in 2023

2023: 2
2015high 2 (2023) · low 0 (2015)2026

Class I Class II/III not classified

FIG. 1 — Life Global Group, LLC by year, 2015–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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