FDA applicant

Holl Meditronics, Inc.

Bolton, Ontario, CA6 decisions1989–19960 recalls

FDA records 6 decisions for Holl Meditronics, Inc. (Bolton, Ontario, CA) from 1989 to 1996: 6 510(k) clearances. Most are in product codes LFL (Instrument, Ultrasonic Surgical) and KNS (Unit, Electrosurgical, Endoscopic (With Or…). 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 Holl Meditronics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Holl Meditronics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Holl Meditronics, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?