FDA applicant

Myocure, Inc.

Glendale, CA15 decisions1982–19880 recalls

FDA records 15 decisions for Myocure, Inc. (Glendale, CA) from 1982 to 1988: 15 510(k) clearances. Most are in product codes HNN (Knife, Ophthalmic) and HMX (Cannula, Ophthalmic). 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, ophthalmic panel, where it files most

How often FDA has decided Myocure, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Myocure, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Myocure, Inc.’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

Myocure, 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?