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

Marina Medical

MARINA MEDICAL INSTRUMENTS, INC. · Model 350-255A · UDI-DI 00840306830358

EXX
0
510(k) clearances
10
Adverse events
1
Recalls
41
Facilities

Description

Supracervical Probe w/Solid Ø5cm Convex Tip & Blue Handle

Recalls

DateFirmReason
2009-04-09Marina Medical Instruments Inc.Marina Medical, Sunrise, FL initiated recall of 46 different 350 series devices and 47 different 270 series products because the material used to manufacture the products was not p

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.