15 results · 31ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

The Solstice OCT System

FDA 510(k)
FDA Class 2 ·Orthopedic

NA

FDA UDI
Richard Wolf GmbH·04055207048597·TEM TUBE SET FOR ERBE INSTRUMENT PVC, for TEM ...

VERIGENE SYSTEM, VERIGENE WARFARIN METABOLISM NUCLEIC ACID TEST

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

AMT G-J TUBE

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

ILAB POLARIS MULTI-MODALITY GUIDANCE SYSTEM

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQK·March 3, 2025

ILAB? POLARIS MULTI-MODALITY GUIDANCE SYSTEM

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQK·May 14, 2026

ASR UNI FEMORAL IMPL SIZE 55

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL·Product code KWA·June 14, 2013

RIGHT-NAV COMPATIBLE DUAL-OFFSET ACCOLADE RASP H

FDA Adverse Event
Malfunction ·STRYKER ORTHOPAEDICS MAHWAH·Product code LXH·June 22, 2011

FENESTRATED BIPOLAR FORCEPS INSTRUMENT

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL, INC·Product code GEI·September 12, 2008

HEMOSIL ACUSTAR HIT-IGG(PF4-H)

FDA Adverse Event
Malfunction ·INSTRUMENTATION LABORATORY CO.·Product code LCO·March 13, 2025

HEMOSIL ACUSTAR HIT-IGG(PF4-H)

FDA Adverse Event
Malfunction ·INSTRUMENTATION LABORATORY CO.·Product code LCO·March 13, 2025

VENTED AUTOFEED HUMIDIFICATION CHAMBER

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTT·May 18, 2018

HEMOSIL ACUSTAR HIT-IGG(PF4-H)

FDA Adverse Event
Malfunction ·INSTRUMENTATION LABORATORY CO.·Product code LCO·June 6, 2025

HEMOSIL ACUSTAR HIT-IGG (PF4-H)

FDA Adverse Event
Malfunction ·INSTRUMENTATION LABORATORY CO.·Product code LCO·April 8, 2025

HEMOSIL ACUSTAR HIT-IGG(PF4-H)

FDA Adverse Event
Malfunction ·INSTRUMENTATION LABORATORY CO.·Product code LCO·March 13, 2025