FDA Device Intelligence
Home › MARINA MEDICAL INSTRUMENTS, INC. › Marina Medical

Marina Medical

MARINA MEDICAL INSTRUMENTS, INC. · Model 200-800 · UDI-DI 00840306823619

EMI
4
510(k) clearances
0
Adverse events
4
Recalls
147
Facilities

Description

Arkansas Novaculite Black Translucent Sharpener (1400 grit US) - 6" X 2" X 1/2"

Recalls

DateFirmReason
2021-04-26Meta C.G.M. SpaSterility issues; single use devices labeled as sterile may not have been adequately sterilized
2021-04-26Meta C.G.M. SpaSterility issues; single use devices labeled as sterile may not have been adequately sterilized
2021-04-26Meta C.G.M. SpaSterility issues; single use devices labeled as sterile may not have been adequately sterilized
2021-04-26Meta C.G.M. SpaSterility issues; single use devices labeled as sterile may not have been adequately sterilized

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.