FDA Device Intelligence
Home › RUMEX INTERNATIONAL CORP. › Rumex

Rumex

RUMEX INTERNATIONAL CORP. · Model 16-111 · UDI-DI 00840159903308

HNX
2
510(k) clearances
11
Adverse events
0
Recalls
84
Facilities

Description

Schocket Double Ended Scleral Depressor, With pocket clip, Length 130 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.