893 results · 35ms · Sources: EU EUDAMED, US FDA

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ONLINE TDM CARBAMAZEPINE

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

CosmoLock Pedicle Screw System

FDA UDI
Kalitec Direct LLC·B07311K0310020·Probe, 1.5 inch Ball, Steffee, Straight, Black

Osseoscrew

FDA UDI
ALPHATEC SPINE, INC.·00811801038655·Osseoscrew Trial Probe, Left

Optimotion Blue CR HCCR Total Knee System

FDA UDI
OPTIMOTION IMPLANTS LLC·B6961014P0319020·CR Tibial Insert, UHMWPE + Vitamin E, Size 3, ...

BOJRAB UNIVERSAL LONG IMLANT, MODEL TBD

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

U-SYSTEMS DIAGNOSTIC ULTRASOUND SYSTEM USI-2000

FDA 510(k)
FDA Class 2 ·Radiology

CHARGING SYSTEM

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 28, 2013

ARCHITECT C4000 ANALYZER

FDA Adverse Event
Malfunction ·ABBOTT MANUFACTURING, INC.·Product code JJE·March 28, 2011

CONTOUR TS TEST STRIPS (50)

FDA Adverse Event
Malfunction ·BAYER HEALTHCARE LLC·Product code NBW·April 15, 2008

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·July 30, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·July 21, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·July 24, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·July 24, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·September 10, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·December 26, 2022

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·September 22, 2022

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·February 7, 2022

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·March 1, 2022

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·February 3, 2022

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·January 31, 2022