Home › Device types › HMY
Keratome, Battery-Powered
FDA product code HMY · Class 1 · Ophthalmic
24
Registered devices
51
Adverse events
2
Recalls
12
510(k) clearances
Devices with this code
MORIA — MORIA SAMORIA — MORIA SAMORIA — MORIA SAMORIA — MORIA SAMORIA — MORIA SAMORIA — MORIA SAMORIA — MORIA SAMORIA — MORIA SAMORIA — MORIA SAMORIA — MORIA SAMORIA — MORIA SAMORIA — MORIA SAMORIA — MORIA SAMORIA — MORIA SAMORIA — MORIA SAMORIA — MORIA SAMORIA — MORIA SAMORIA — MORIA SAMORIA — MORIA SAMORIA — MORIA SAMORIA — MORIA SAMORIA — MORIA SAMORIA — MORIA SAMORIA — MORIA SA
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2007-08-09 | Becton Dickinson and Company | Microkeratome blade may stop oscillating and transverse the eye causing injury to the cornea |
| 2003-01-24 | BD Opthalmic Systems | Microkeratome Blade may cause irregular corneal flap which may delay patients procedure. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.