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

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SAS SHIGELLA BOYDII TYPE 10 ANTISERUM

FDA 510(k)
FDA Class 2 ·Microbiology

P.F.C. SIGMA

FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295239611·P.F.C. SIGMA TC3 TIBIAL INSERT TRIAL SZ 5 20mm ...

De Soutter Medical

FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471149830·K-WIRE - DOUBLE TROCAR FULLY THREADED 1.5mm DIA...

ENDOFLATOR 40, ENDOFLATOR 50

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

MEPILEX AG ABSORBENT SILICONE-COATED DRESSING

FDA 510(k)
FDA Unclassified ·Unknown

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code GCL·February 28, 2022

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code GCL·October 26, 2022

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code GCL·August 22, 2022

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code GCL·November 28, 2023

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code GCL·April 18, 2023

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code GCL·September 25, 2024

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code GCL·October 15, 2025

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code GCL·October 1, 2024

EXPRESS® SD RENAL/BILIARY

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code FGE·February 14, 2013

UNICEL® DXC 600 PRO SYNCHRON® CLINICAL SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code JJE·January 14, 2011

POWERED WHEELCHAIR

FDA Adverse Event
Malfunction ·INVACARE TAYLOR STREET·Product code ITI·July 28, 2014

PROXIMATE LINEAR CUTTER

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GCJ·October 23, 1996