44 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DEPUY GLOBAL UNITE SHOULDER SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
TAMPAX PEARL SCENTED AND UNSCENTED TAMPONS - JUNIOR, REGULAR, SUPER & SUPER PLUS
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
HT III SA FIXTURE SYSTEM
FDA 510(k)
FDA Class 2
·Dental
TI-SCREW FULL THD 6 X 60
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code HSB·November 11, 2015
CARPENTIER-EDWARDS BIOPROSTHESIS
FDA Adverse Event
Injury
·BAXTER HEALTHCARE CORP.·Product code LWR·February 27, 1997
SUSTAIN 4X13 HA CYLINDER IMPLANT
FDA Adverse Event
Injury
·LIFECORE BIOMEDICAL, INC.·Product code DZE·December 30, 1998
SPECTRUM CONTOUR POST-OPERATIVELY ADJUSTABLE MAMMARY PROSTHE
FDA Adverse Event
Injury
·MENTOR·Product code FWM·October 12, 1998
ARTIFICIAL URINARY SPHINCTER
FDA Adverse Event
Injury
·AMERICAN MEDICAL SYSTEMS, INC.·Product code EZY·October 24, 1997
TSRH SPINAL FIXATION SYSTEM
FDA Adverse Event
Injury
·SOFAMOR DANEK MANUFACTURING·Product code KWP·May 19, 1999
ZYPLAST COLLAGEN IMPLANT
FDA Adverse Event
Injury
·COLLAGEN CORP.·Product code LMH·December 27, 1996
PREC O/L INS 28MM 10_P2
FDA Adverse Event
Malfunction
·HOWMEDICA INC.·Product code KWB·January 23, 1998
MAYFIELD SKULL CLAMP
FDA Adverse Event
Other
·OHIO MEDICAL INSTRUMENT·Product code HBL·April 21, 1998
TRUWAVE
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES DR·Product code DXO·May 28, 2026
TRUWAVE
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES DR·Product code DXO·April 22, 2026
SYNCHROMED
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code LKK·March 17, 1999
ACROMED VSP SCREW
FDA Adverse Event
Injury
·ACROMED CORP·Product code JDN·September 1, 1998
INFUSAID IMPLANTABLE INFUSION PUMP
FDA Adverse Event
Injury
·STRATO/INFUSAID, INC.·Product code MDY·July 10, 1997
COATED VICRYL (P0LYGLACTIN 910) SUTURE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code GAM·August 27, 2004
ZYPLAST COLLAGEN IMPLANT
FDA Adverse Event
Injury
·COLLAGEN CORP.·Product code LMH·February 19, 1999
ACTICON NEOSPHINCTER
FDA Adverse Event
Injury
·AMERICAN MEDICAL SYSTEMS, INC.·Product code EZY·August 26, 2013