21 results · 22ms · Sources: EU EUDAMED, US FDA

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SGS ECCOVISIONTM Pharyngometer, SGS ECCOVISIONTM Rhinometer, SGS ECCOVISIONTM Rhino/Pharyngometer

FDA 510(k)
FDA Class 2 ·Anesthesiology

Polysorb

FDA UDI
Covidien LP·20884521126784·Absorbable Single Stitch Reload

Bernafon

FDA UDI
Bernafon AG·05711584062999·SA5 IIC, V2 BL SAPHIRA 5

OsteoMed

FDA UDI
OSTEOMED LLC·00845694004671·SpectrumTM Short Left Maxillary Plate Assembly

OMNIGUIDE ZERO FLOW ZF-T WAVEGUIDE FIBER

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

EMCOOLSPAD

FDA 510(k)
FDA Class 2 ·Cardiovascular

Widex

FDA UDI
Widex A/S·05706069787689·WIDEX EVOKE E-FM (Cappuccino brown ) 30, RC coil

Widex

FDA UDI
Widex A/S·05706069897685·WIDEX EVOKE E-FP (Cappuccino brown ) 30, Teleco...

Widex

FDA UDI
Widex A/S·05706069896022·WIDEX EVOKE E-FA (Cappuccino brown ) 30, Teleco...

ENDO STITCH

FDA Adverse Event
Injury ·DAVIS & GECK CARIBE LTD·Product code OCW·August 15, 2023

Covidien EndoStitch" Polysorb Single Use Loading Unit; Product numbers: 170053 and 170071;

FDA Enforcement
Class II ·Ongoing·Covidien, LP·June 10, 2026

ENDO GIA II 60-4.8 SULU

FDA Adverse Event
Injury ·USSC PUERTO RICO·Product code GDW·July 13, 2011

EEA 28MM SINGLE-USE STAPLER

FDA Adverse Event
Injury ·COVIDIEN·Product code GDW·June 4, 2013

FLO-GARD 6201 VOLUMETRIC INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE·Product code FRN·September 24, 2008

Covidien EndoStitch" Polysorb Single Use Loading Unit; Product numbers: 170053 and 170071;

FDA Recall
Open, Classified ·Product code OCW·April 15, 2026

ACETABULAR SIZER SIZE 48MM

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code KXA·August 17, 2021

HEARTMATE 3 VAD MODULAR CABLE

FDA Adverse Event
Malfunction ·THORATEC CORPORATION·Product code DSQ·August 18, 2021

REDUC-FORC W/POINT SOFTLO L161

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HTD·September 12, 2022

REDUC-FORC W/POINT SOFTLO L161

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HTD·March 31, 2021

REDUC-FORC W/POINT SOFTLO L161

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HTD·September 20, 2022