73 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AZUR DETACHABLE 35 PLATINUM COIL SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450169087·
Cadet Cervical Cage
FDA UDI
VALORUS SPINE LLC·00811771033803·Cadet Cervical Cage, 11mm x 13mm x 07mm, 7° Lor...
Cadet Cervical Cage
FDA UDI
VALORUS SPINE LLC·00811771033179·Cadet Cervical Cage, 11mm x 13mm x 07mm, Non-Lo...
K2M General Instruments
FDA UDI
VB Spine LLC·10888857531024·Trial Size 14x17x6 mm, 6°
MIDWEST REPROCESSING CENTER REPROCESSED LNCS SESSORS; MIDWEST REPROCESSING CENTER REPROCESSED OXIMAX SENSORS; MIDWEST RE
FDA 510(k)
FDA Class 2
·Cardiovascular
BLOOD GLUCOSE MONITORING SYSTEM, MODELS AG-6081 AND AG-6951
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Anterior Cervical IBFD
FDA UDI
KEOS·B084AC1111307000·
Anterior Cervical IBFD
FDA UDI
KEOS·B084AC1111307070·
Anterior Cervical IBFD
FDA UDI
KEOS·B084AC1111307040·
UNKNOWN PATHINDER NXT OR INSTINCT JAVA IMPLANT
FDA Adverse Event
Malfunction
·ZIMMER BIOMET SPINE INC.·Product code NKB·September 24, 2022
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·May 14, 2013
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
Malfunction
·INVAMEX·Product code IOR·September 23, 2014
LD304 MATERNITY BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code HDD·May 18, 2011
TL PEDICLE SCREW DIA. 6,5 LG 50
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 50
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 35
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code HWC·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 40
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 45
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 35
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019