FDA Device Intelligence
HomeSONTEC INSTRUMENTS, INC. › BUCK EAR CURETTE

BUCK EAR CURETTE

SONTEC INSTRUMENTS, INC. · Model 467-386 · UDI-DI 00192896039773

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

Description

BUCK EAR CURETTE ANGLED BLUNT END SIZE 2 ROUND HANDLE

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.