FDA Device Intelligence
HomeMARINA MEDICAL INSTRUMENTS, INC. › Marina Medical

Marina Medical

MARINA MEDICAL INSTRUMENTS, INC. · Model 020-044 · UDI-DI 00840306830280

FNY
9
510(k) clearances
11
Adverse events
1
Recalls
224
Facilities

Description

Deep Pelvic Tray, Blue Perforated Lid, 58cm x 28cm x 15cm

Recalls

DateFirmReason
2023-05-30DeRoyal Industries IncThe outer package seal could be open, or compromised which affects the sterility of the procedure pack inside.

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 docs
Data 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.