27 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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