510(k) Report

FDA applicant

(Arms) Hoffman Surgical Equipment, Ivf Division

Conshohocken, PA1 decision1999–19990 recalls

FDA records 1 decision for (Arms) Hoffman Surgical Equipment, Ivf Division (Conshohocken, PA) in 1999: 1 510(k) clearance. All are in product code MQG (Accessory, Assisted Reproduction). 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 (Arms) Hoffman Surgical Equipment, Ivf Division’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for (Arms) Hoffman Surgical Equipment, Ivf Division since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — (Arms) Hoffman Surgical Equipment, Ivf Division by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • MQGAccessory, Assisted Reproduction1decision

What has FDA decided for it lately?

  • K991216Hoffman Ivf-1(Arms) Hoffman Surgical Equipment, Ivf Division · 1999

The one decision as (Arms) Hoffman Surgical Equipment, Ivf Division →