Home › MARINA MEDICAL INSTRUMENTS, INC. › Marina Medical
Marina Medical
MARINA MEDICAL INSTRUMENTS, INC. · Model 042-042 · UDI-DI 00840306836282
10
510(k) clearances
49
Adverse events
1
Recalls
719
Facilities
Description
Bowman Lacrimal Duct Probe, 0.9/1.1mm , 1-2
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2008-06-05 | Phillips Safety Products | Radiation Protective Eyewear does not meet the radiation protection levels stated on the labeling. |
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 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.