23 results · 30ms · Sources: EU EUDAMED, US FDA

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EDWARDS LIFESCIENCES INTRACLUDE INTRA-AORTIC CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

NexxZr™ T / D-100-30-NT-D400-SD

FDA UDI
SAGEMAX BIOCERAMICS, INC·00842271113856·

Clear Readers

FDA UDI
Diversified Products, Inc.·00037741113232·

Reef TH

FDA UDI
Seaspine Orthopedics Corporation·10889981201012·Interbody, 11mm x 32mm x 17mm, 15 deg

Reef TA

FDA UDI
Seaspine Orthopedics Corporation·10889981208134·Trial, 11mm x 32mm x 17mm, 15 deg

GERBODE NEEDLE HOLDER

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896075863·GERBODE NEEDLE HOLDER TUNGSTEN CARBIDE SERRATED...

Reef TA

FDA UDI
Seaspine Orthopedics Corporation·10889981193027·Interbody, 11mm x 32mm x 17mm, 15 deg

Reef TO

FDA UDI
Seaspine Orthopedics Corporation·10889981204860·Trial, 11mm x 32mm x 17mm, 15 Deg

Reef TO

FDA UDI
Seaspine Orthopedics Corporation·10889981190712·Interbody, 11mm x 32mm x 17mm, 15 Deg

RAPIDVUE HCG TEST

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

DESENS-IONOMER

FDA 510(k)
FDA Class 2 ·Dental

ONE TOUCH ULTRA

FDA Adverse Event
Malfunction ·LIFESCAN, INC.·Product code CFR·July 25, 2002

OPTISITE ARTERIAL CANNULA

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code DQR·June 21, 2024

GENISTRONG

FDA Adverse Event
Malfunction ·GENICON·Product code GCJ·October 15, 2017

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 1, 2014

ACCU-CHEK ® TENDER INFUSION SET

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·May 29, 2013

UNKNOWN PRODUCT

FDA Adverse Event
Other ·STRYKER ORTHOPAEDICS CORK·Product code MRA·June 6, 2011

OPTISITE ARTERIAL CANNULA

FDA Adverse Event
Malfunction ·EDWARDS LIFESCIENCES·Product code DQR·June 21, 2024

SWARTZ¿ INTRODUCER, UNKNOWN

FDA Adverse Event
Injury ·ST. JUDE MEDICAL·Product code DYB·March 25, 2020

AGILIS¿ INTRODUCER, UNKNOWN

FDA Adverse Event
Death ·ST. JUDE MEDICAL, COSTA RICA LTDA·Product code DYB·March 25, 2020