44 results · 24ms · Sources: EU EUDAMED, 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