47 results
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35ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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VISERA 4K UHD SYSTEM
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
n.a.
FDA UDI
Karl Storz GmbH & Co. KG·04048551001325·Cotton Applicator, standard, Ø 1.1mm
AGXO
FDA UDI
Oticon A/S·05707131283498·H100V2, BTE 13 WL 85 CBE AGXO
AGC Tradition Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304240483·
BrightGear Headgear
FDA UDI
ORMCO CORPORATION·00889989079937·WEBBING, HIGH PULL BLACK
OsteoMed
FDA UDI
OSTEOMED LLC·00845694040662·PrimaLIF LLIF 11mm x 18mm Lordotic Trial
ihc Enhancer Kit, 30mL
FDA UDI
NOVODIAX, INC.·00850000596528·
ihc Enhancer Kit, 15mL
FDA UDI
NOVODIAX, INC.·00850000596511·
ihc Enhancer 5mL
FDA UDI
NOVODIAX, INC.·00850030934598·
ihc Enhancer 15mL
FDA UDI
NOVODIAX, INC.·00850030934604·
VARIANT
FDA UDI
CAMBER SPINE TECHNOLOGIES, LLC·B030SPO1510110·Threaded Fixation Pin, 110mm
5.1MHZ PENCIL PROBE
FDA UDI
PARKS MEDICAL ELECTRONICS, INC.·00816787020724·
NA
FDA UDI
aap Implantate AG·04042409192333·Cortical Screw 1.5, self-tapping, L 11
ENDOSSEOUS DENTAL IMPLANT ABUTMENT
FDA 510(k)
FDA Class 2
·Dental
HI-TORQUE BALANCE MIDDLEWEIGHT UNIVERSAL
FDA 510(k)
FDA Class 2
·Cardiovascular
NA
FDA UDI
aap Implantate AG·04042409192470·Cortical Screw 1.5, self-tapping, L 11
SIGNATURE Head - CoCr
FDA UDI
AMPLITUDE SAS·03701089520577·
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code NAY·January 11, 2019
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code NAY·January 11, 2019
AMISTEM H COLLARED FEMORAL STEMS
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·February 12, 2026