27 results · 41ms · Sources: EU EUDAMED, US FDA

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ERCH ARCH BAR, MODEL 38-690-00

FDA 510(k)
FDA Class 2 ·Dental

POWDER-FREE LATEX EXAMINATION GLOVE, BLUE COLORED

FDA 510(k)
FDA Class 1 ·General Hospital

SAMARCO SPIDER PLATES

FDA 510(k)
FDA Class 2 ·Orthopedic

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·January 21, 2026

VENTURE ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC SOFAMOR DANEK PUERTO RICO OPERATIONS·Product code KWQ·December 2, 2011

VENTURE ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code KWQ·April 16, 2018

VENTURE ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·October 30, 2009

VENTURE ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWQ·October 7, 2015

VENTURE ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWQ·September 11, 2019

VENTURE ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWQ·September 11, 2019

VENTURE ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWQ·October 9, 2019

VENTURE ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWQ·October 11, 2019

VENTURE ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWQ·September 11, 2019

VENTURE ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code HWC·October 29, 2009

VENTURE ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWQ·January 3, 2013

VENTURE ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC SOFAMOR DANEK PUERTO RICO OPERATIONS·Product code KWQ·August 12, 2011

UNICEL® DXI 800 ACCESS® IMMUNOASSAY SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER·Product code DHA·April 16, 2013

FREESTYLE

FDA Adverse Event
Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·June 19, 2008

6.2MM TI CLICK'X PEDICLE SCREW DUAL CORE 40MM THREAD LENGTH

FDA Adverse Event
Injury ·SYNTHES MONUMENT·Product code NKB·April 11, 2011

VENTURE ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWQ·December 11, 2009