FDA Device Intelligence
HomeNORTH EOS INDUSTRIES INC. › EOS

EOS

NORTH EOS INDUSTRIES INC. · Model EosCurette-RING BLUE · UDI-DI 04712568360514

JYG Prescription
7
510(k) clearances
27
Adverse events
1
Recalls
148
Facilities

Description

EOS DISPOSABLE EAR CURETTE-RING BLUE

Recalls

DateFirmReason
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.

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.