17 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Suture, Nonabsorbable, Silk
FDA Pre-Market Approval
FDA Class 2
·NONABSORBABLE SURG. SUTURES, BRAIDED SILK
Suture, Nonabsorbable, Silk
FDA Pre-Market Approval
FDA Class 2
·NONABSORBABLE SURG. SUTURES, BRAIDED SILK
Suture, Nonabsorbable, Silk
FDA Pre-Market Approval
FDA Class 2
·NONABSORBABLE SURG. SUTURES, BRAIDED SILK
Suture, Nonabsorbable, Silk
FDA Pre-Market Approval
FDA Class 2
·NONABSORBABLE SURG. SUTURES, BRAIDED SILK
Suture, Nonabsorbable, Silk
FDA Pre-Market Approval
FDA Class 2
·NONABSORBABLE SURG. SUTURES, BRAIDED SILK
Suture, Nonabsorbable, Silk
FDA Pre-Market Approval
FDA Class 2
·NONABSORBABLE SURG. SUTURES, BRAIDED SILK
VANGUARD(TM)
FDA UDI
Biomet Orthopedics, LLC·00880304444928·
Vanguard®
FDA UDI
Biomet Orthopedics, LLC·00887868492495·
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·August 6, 2015
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·August 6, 2015
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·April 10, 2025
ONE TOUCH BASIC
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·February 5, 2002
CUSTOM MRS DISTAL FEMORAL STEM
FDA Adverse Event
Injury
·HOWMEDICA OSTEONICS·Product code JDI·June 26, 2000
ACCUCHEK INSTANT
FDA Adverse Event
Injury
·BOEHRINGER MANNHEIM CORP.·Product code CFR·August 26, 1998
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·December 23, 2010
Promote Quadra, Sterile EO, Model # / Part #: CD3221-36/100025054, 60019195; CD3223-36P/100013763; CD3239-40/100029115, 100029254, 100037181; CD3239-40Q/100029116, 100029244, 100037115
FDA Enforcement
Class II
·Terminated·St Jude Medical Inc.·July 4, 2018
Pump 371 14F LT CMR Set; Product Code: 0048-0045;
FDA Enforcement
Class II
·Ongoing·Abiomed, Inc.·September 11, 2024