FDA applicant

Raymart Development Co.

Atlanta, GA1 decision1994–19940 recalls

FDA records 1 decision for Raymart Development Co. (Atlanta, GA) in 1994: 1 510(k) clearance. All are in product code HGE (Amniotome). 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 Raymart Development Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Raymart Development Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Raymart Development Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

See the 510(k) Report

Raymart Development Co.

Which product codes does it file in?

What has FDA decided for it lately?