510(k) Report

FDA applicant

Aslan Medical Technologies, Ltd.

Kalamazoo, MI8 decisions1992–19980 recalls

FDA records 8 decisions for Aslan Medical Technologies, Ltd. (Kalamazoo, MI) from 1992 to 1998: 8 510(k) clearances. Most are in product codes GCJ (Laparoscope, General & Plastic Surgery) and FDE (Laparoscopy Kit). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Aslan Medical Technologies, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Aslan Medical Technologies, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Aslan Medical Technologies, Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Aslan Medical Technologies, Ltd.’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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