24 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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STRYKER TITANIUM CROSS-SCREW SYSTEM, MODEL 234-500-1XX
FDA 510(k)
FDA Class 2
·Orthopedic
Zirlux
FDA UDI
HENRY SCHEIN, INC.·H65890113190·Zirlux Titanium Blank Abutment compatible with:...
N/A
FDA UDI
BIOMET MICROFIXATION, INC·00841036008734·
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0113100·Decorticating Planer
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033316313·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033316320·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033316344·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033316337·
K091319
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·January 9, 2026
INSET 30
FDA Adverse Event
Injury
·UNOMEDICAL UM-D·Product code FPA·November 12, 2025
BRACHYSEED PD-103 MODELS #PD1
FDA 510(k)
FDA Class 2
·Radiology
XIA SPINE SYSTEM HOOKS
FDA 510(k)
FDA Class 2
·Orthopedic
OneLIF™
FDA UDI
Novapproach Spine LLC·G07001131920100·Trial-OneLIF Interbody, Large, 19 Degree, 20mm ...
OneLIF™
FDA UDI
Novapproach Spine LLC·G07001131916060·Trial-OneLIF Interbody, Large, 19 Degree, 16mm ...
OneLIF™
FDA UDI
Novapproach Spine LLC·G07001131918080·Trial-OneLIF Interbody, Large, 19 Degree, 18mm ...
INSET 30
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·September 4, 2025
INFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code MEB·September 17, 2021
INFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code MEB·September 4, 2024
INFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·May 14, 2018
ENDOPATH ETS FLEX
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.·Product code KOG·February 6, 1998