# Myocure, Inc.

- Location (FDA's records): Glendale, CA
- FDA decisions: 15 (1982–1988): 15 510(k) clearances
- Product codes: HNN (5), HMX (2), HMR (1), HNY (1), IYO (1), HMN (1), HNC (1), FZZ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Lensx Lasers, Inc.: 1 (https://510kreport.com/company/lensx-lasers)

## Its most-cited devices
- K853598: Ophthalmic Knife W/Removale Depth Guide (1985), cited by 1

## Recent decisions
- K880346: Cannulas (May 3, 1988)
- K880347: Anesthesia/Retrobulbar Needles (May 3, 1988)
- K880345: Cystotomes/Knifes (May 3, 1988)
- K874057: Ophthalmic Tip & Blade Scalpels (Dec 23, 1987)
- K874056: Ophthalmic Disposable Blades (Dec 22, 1987)
- K873385: Ophthalmic Phaco-Blade (Sep 21, 1987)
- K864371: Surgical Skin Marker (Nov 17, 1986)
- K863662: Ophthalmic Surgical Drape (Oct 20, 1986)

Source page: https://510kreport.com/company/myocure