29 results · 25ms · Sources: EU EUDAMED, US FDA

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4-WEB CERVICAL STS (SPINAL TRUSS SYSTEM)

FDA 510(k)
FDA Class 2 ·Orthopedic

NOVO Health Services, LLC

FDA UDI
NOVO HEALTH SERVICES, LLC·00812564032362·400 CC SMALL BASIN

Z Liquid ST C4-S 100ml

FDA UDI
ARGEN CORPORATION, THE·D818121741·Dental porcelain/ceramic restoration kit

23 G X 1 IN. BD INTEGRA¿ 3 ML SYRINGE WITH DETACHABLE NEEDLE

FDA Adverse Event
Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·November 7, 2017

23 G X 1 IN. BD INTEGRA¿ 3 ML SYRINGE WITH DETACHABLE NEEDLE

FDA Adverse Event
Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code MEG·November 7, 2017

DIATRON PICTUS 400

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

CRITERTION, MODEL #1067511

FDA 510(k)
FDA Class 2 ·Dental

ASR UNI FEMORAL IMPL SIZE 53

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL·Product code KWA·May 21, 2013

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·September 26, 2014

WECK HEM-O-LOK ENDO APPLIER

FDA Adverse Event
Malfunction ·TELEFLEX MEDICAL·Product code FZP·May 20, 2011

PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code MGB·April 14, 2016

PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code MGB·April 14, 2016

PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code MGB·April 14, 2016

PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code MGB·April 14, 2016

PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code MGB·April 14, 2016

PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code MGB·April 14, 2016

PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code MGB·April 14, 2016

StarClose SE Vascular Closure System, Part No. 14679-01, 14679-02. The UDI is 08717648079467. The GMDN is 47411.

FDA Enforcement
Class II ·Terminated·Abbott Vascular·February 22, 2017

GYNECARE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code OTO·July 27, 2018

2210968-2018-74702

FDA Adverse Event
Injury ·July 29, 2018