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

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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