27 results · 24ms · Sources: EU EUDAMED, US FDA

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Nexta PEEK Hammertoe Correction 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

ELITECH CLINICAL SYSEMS ISE CONTROL 1 AND 2

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

SILASTIC (R) GREAT TOE IMPLANT H.P. (SWANSON DESIGN)

FDA Adverse Event
Injury ·DOW CORNING CORP·Product code KWD·October 16, 1996

TSRH SPINAL FIXATION SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK MANUFACTURING·Product code KWQ·August 3, 2000

BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX SYSTEM

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code QJR·May 18, 2021

AUTO SUTURE CHEMOSITE MINI CATHETER POLYURETHANE SYSTEM

FDA Adverse Event
Injury ·UNITED STATES SURGICAL CORPORATION·Product code LJT·September 5, 1997

ACHIEVER BALLOON DILATATION CATHETER

FDA Adverse Event
Injury ·MICROVASIVE ENDOSCOPY A DIV OF BOSTON SCIENTIFIC CORP.·Product code KNQ·May 4, 1998

ORBIS SIGMA VALVE

FDA Adverse Event
Injury ·ELEKTA IMPLANTS SA·Product code JXG·May 15, 1998

ALTA TRAN/TIB/HUM/SC 3.7X30MM

FDA Adverse Event
Malfunction ·HOWMEDICA, INC.·Product code HSB·December 11, 1997

ZYPLAST COLLAGEN IMPLANT

FDA Adverse Event
Injury ·COLLAGEN CORP.·Product code LMH·October 10, 1997

UNK DEVICE

FDA Adverse Event
Injury ·UNK·Product code GAG·August 27, 1998

GORE TEX

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES, INC.·Product code MCI·September 10, 1996

INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 29, 2014

NUVASIVE LATERAL PLATE SYSTEM

FDA Adverse Event
Malfunction ·NUVASIVE, INC.·Product code KWQ·July 8, 2011

PK DISSECTING FORCEPS INSTRUMENT

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·July 8, 2013

PALMAZ SCHATZ BALLOON EXPANDABLE STENT WITH DELIVERY SYSTEM

FDA Adverse Event
Injury ·CORDIS, A JOHNSON AND JOHNSON CO·Product code MAF·April 15, 1998

PALMAZ SCHATZ BALLOON EXPANDABLE STENT WITH DELIVERY SYSTEM

FDA Adverse Event
Injury ·CORDIS, A JOHNSON AND JOHNSON CO·Product code MAF·April 15, 1998

ENDOPATH TRISTAR EXTRAPERITONEAL DISSECTOR

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, INC.·Product code GCJ·July 10, 1997

EPIDURAL CATHETER

FDA Adverse Event
Injury ·ABBOTT LABORATORIES·Product code BSO·October 16, 1998