328 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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M2 NAVIGATION CATHETER AND GUIDELINER NAVIGATION CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
DP-Tray-R
FDA UDI
Denplus Inc·D8451112100·DP-Tray-R. Liquid for Premium Tray, 240 ml
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702274790·ELVAREX 3/THIGH HIGH/CLOSED TOE, E-VERSION, KNE...
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702256871·Elvarex 2/Thigh High/Slant, Closed Toe, E-Versi...
Integrity-SI Fusion System
FDA UDI
Lincotek Medical LLC·B57112521112100D0·12 x 100 mm Anodized SI Implant Fully Threaded
MetaSystems Probes
FDA UDI
MetaSystems Probes GmbH·04251315818583·XL t(14;16) IGH/MAF DF, Translocation/Dual Fusi...
Coated Revision Stem
FDA UDI
SIGNAL MEDICAL CORPORATION·B046220811121000·12x100 Coated Revision Stem
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07310K0121000·Tb Breaker, Tower Tab, MIS
Alliant Biotech
FDA UDI
MEDISURGE LLC·G611220811121000·Symmetric Total Knee Coated Revision Stem Size ...
MAC-LAB SYSTEM, CARDIOLAB SYSTEM, COMBOLAB SYSTEM, SPECIALSLAB SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
ENCOR ENSPIRE BREAST BIOPSY SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
IMP TM 4.7MM MTX FULL, 11.5MM
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·November 25, 2022
IMP TM 4.7MM MTX FULL, 10
FDA Adverse Event
Injury
·ZIMVIE US CORP LLC·Product code DZE·April 23, 2026
IMP TM 4.7MM MTX FULL, 10
FDA Adverse Event
Injury
·ZIMVIE US CORP LLC·Product code DZE·April 23, 2026
LIFEVEST WCD 4000
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·May 3, 2013
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·September 23, 2014
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·June 2, 2011
IMP TM 4.1MM MTX FULL, 11.5MM
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·June 1, 2020
OSIGRAFT (EPTOTERMIN ALFA)
FDA Adverse Event
OLYMPUS BIOTECH·Product code MPY·May 24, 2012
IMP TM 4.1MM MTX FULL,10M
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·July 2, 2021