188 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Lympha Press Optimal Plus
FDA 510(k)
FDA Class 2
·Cardiovascular
OsteoMed
FDA UDI
OSTEOMED LLC·00845694005388·90mm x 90mm Malleable Osteoform Mesh Plate
IN-OVATION® R
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K189003001·IN-OVATION® R Pickard RX Adolescent KIT
OsteoMed
FDA UDI
OSTEOMED LLC·00845694005395·90 x 90mm Malleable Osteoform Mesh, Sterile
XPRESS BALLOON DEVICE
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
VANTAGE TITAN HSR
FDA 510(k)
FDA Class 2
·Radiology
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304817951·
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304817968·
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304817982·
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304817937·
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304817944·
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304817975·
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 28, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 24, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 28, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·November 7, 2021
VENTAK PRIZM 2 DR
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS, INC·Product code LWS·August 10, 2004
THERMOPHORE
FDA Adverse Event
Injury
·BATTLE CREEK EQUIPMENT CO.·Product code IRT·June 23, 2017
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·August 11, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 29, 2021