FDA Device Intelligence
Home › RUMEX INTERNATIONAL CORP. › Rumex

Rumex

RUMEX INTERNATIONAL CORP. · Model 20-202 · UDI-DI 00840159908020

HND
6
510(k) clearances
90
Adverse events
0
Recalls
161
Facilities

Description

FemtoLASIK Flap Spatula, Length 121 mm, Round Titanium Handle

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.