6 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
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RESTORIS POROUS PARTIAL KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer
FDA classification
FDA Class 2
·Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer
HES ULTRASONIC THERAPY APPLIANCE, MODELS HS-3008 (1MHZ), HS3026 (2MHZ), HS-3040 (3MHZ)
FDA 510(k)
FDA Class 2
·Physical Medicine
PIEZOELECTRIC SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Instrument, Surgical, Sonic And Accessory/Attachment
FDA classification
FDA Class 2
·Instrument, Surgical, Sonic And Accessory/Attachment
Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat
FDA classification
FDA Class 2
·Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat