MORIA
MORIA SA · Model M2 SUCTION RING -1 · UDI-DI 03700483608331
HMY
Prescription
10
510(k) clearances
51
Adverse events
2
Recalls
5
Facilities
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. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.