14 results · 18ms · Sources: EU EUDAMED, US FDA

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IMX TOTAL B-HCG

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

REVELATION DIAMOND

FDA UDI
Ss White Burs, Inc.·D6909125352·REVELATION DIAMOND 850-014F - 5 PACK

Gen. Acces/ Instr. Tip Guard

FDA UDI
KATENA PRODUCTS, INC.·00841668110898·TIP GUARDS VENTED YELLOW PACK OF 100

Gen. Acces/ Instr. Tip Guard

FDA UDI
KATENA PRODUCTS, INC.·00841668110874·TIP GUARDS VENTED GREEN PACK OF 100

Unity

FDA UDI
DIOMEDICAL CO.,LTD.·08800113960282·Unity Sacroiliac Joint Fixation - Threaded Coun...

HNM MEDICAL

FDA UDI
HNM STAINLESS, LLC.·00842962159286·BLUNT OBTURATOR FOR 3.4MM OPERATING SHEATH 0° T...

GENESIS REUSABLE RIGID CONTAINER SYSTEM

FDA 510(k)
FDA Class 2 ·General Hospital

DRG DISPOSABLE VAGINAL SPECULUM

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

HEARTSTART ONSITE

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 14, 2014

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 13, 2013

COLLEAGUE CX VOLUMETRIC INFUSION PUMP SINGLE CHANNEL

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·December 2, 2010

DATASCOPE MR MONITOR

FDA Adverse Event
Malfunction ·DATASCOPE CORP./PT MONITORING DIVISION·Product code MHX·January 23, 2003

PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code HSX·October 15, 2025

GENESIS UNI KNEE FEMORAL COMPONENT COCR

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code HSX·May 23, 2025