197 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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KFX PEEK BONE ANCHOR WITH PRE-ATTACHED SUTURES AND INSERTER HANDLE
FDA 510(k)
FDA Class 2
·Orthopedic
Harvard Bond SE Mono
FDA UDI
Harvard Dental International GmbH·EHAR70836091·Light cure self-etching one component adhesive
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K0830090·Persuader, Rod Reduction, Kerrison Type
ZAVATION
FDA UDI
Zavation LLC·00842166154865·WHITNEY 8deg 36mmx9mm
Zavation
FDA UDI
Zavation LLC·00842166106093·ALIF 8deg 36mmx09
Zavation
FDA UDI
Zavation LLC·00842166180536·ALIF Sizer 8deg 36mm x 9mm
ZAVATION
FDA UDI
Zavation LLC·00842166157088·HA+ ALIF 8deg 36mmx9
N-MID OSTEOCALCIN ONE STEP ELISA MODEL 30SC4000
FDA 510(k)
FDA Class 2
·Clinical Chemistry
NEXUS 2 CLEAR
FDA 510(k)
FDA Class 2
·Dental
STAYFUSE FUSION SYSTEM
FDA Adverse Event
Other
·NEXA ORTHOPEDICS, INC.·Product code HWC·February 14, 2006
INFUSOMAT®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FRN·April 11, 2025
INFUSOMAT®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FRN·May 11, 2026
INFUSOMAT®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FRN·April 7, 2026
INFUSOMAT®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FRN·April 3, 2026
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·April 29, 2013
STERLING BALLOON DILATATION CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQY·May 10, 2011
CELL-DYN WBC REAGENT A
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·July 29, 2008
INFUSOMAT®
FDA Adverse Event
Malfunction
·B.BRAUN MELSUNGEN AG·Product code FRN·April 30, 2026
INFUSOMAT®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FRN·May 19, 2025
INFUSOMAT®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FRN·May 1, 2025