FDA applicant

Autosafe-Refelx, Inc.

Alpharetta, GA1 decision2007–20070 recalls

FDA records 1 decision for Autosafe-Refelx, Inc. (Alpharetta, GA) in 2007: 1 510(k) clearance. All are in product code FMI (Needle, Hypodermic, Single Lumen). 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 Autosafe-Refelx, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2007

2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Autosafe-Refelx, Inc.’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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Other applicant names beginning “Autosafe-Refelx”

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

Autosafe-Reflex, Inc. 1

Autosafe-Refelx, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Autosafe-Refelx”