36 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MODIFICATION TO STEATHSTATION TREATMENT GUIDANCE PLATFORM
FDA 510(k)
FDA Class 2
·Neurology
Creation Willi Geller
FDA UDI
KLEMA Dentalprodukte GmbH·ECWG0011531·In Nova Neo INN-3 yellow
artVeneer life
FDA UDI
Merz Dental GmbH·D7092001153·artVeneer life lower anteriors, UCM, A4
UniPlex
FDA UDI
Pajunk GmbH Medizintechnologie·14048223018061·UniPlex
UP 3/1...
UniPlex
FDA UDI
Pajunk GmbH Medizintechnologie·14048223018054·UniPlex
UP 3/2...
UniPlex
FDA UDI
Pajunk GmbH Medizintechnologie·14048223019501·UniPlex
UP 3/4...
UNIPLEX®
FDA UDI
Pajunk GmbH Medizintechnologie·04048223049242·001153-74
UniPlex
FDA UDI
Pajunk GmbH Medizintechnologie·14048223015558·UniPlex
UP 3/8...
UniPlex
FDA UDI
Pajunk GmbH Medizintechnologie·14048223015589·UniPlex
UP 3/1...
UNIPLEX®
FDA UDI
Pajunk GmbH Medizintechnologie·04048223049228·001153-71
UNIPLEX®
FDA UDI
Pajunk GmbH Medizintechnologie·04048223102459·001153-70
Uniplex UP
FDA UDI
Pajunk GmbH Medizintechnologie·14048223017378·Uniplex UP
UP 3/1...
UNIPLEX®
FDA UDI
Pajunk GmbH Medizintechnologie·04048223049259·001153-77
UniPlex
FDA UDI
Pajunk GmbH Medizintechnologie·14048223015572·UniPlex
UP 3/5...
UNIPLEX®
FDA UDI
Pajunk GmbH Medizintechnologie·04048223049266·001153-82
QUICK SET
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A DE C.V·Product code FPA·May 14, 2026
ARTHRO-SURGIMAT-A103
FDA 510(k)
FDA Class 2
·Orthopedic
WIRELESS AMBULATORY EEG, MODEL EX-AMB-WIRELESS (PROPOSED)
FDA 510(k)
FDA Class 2
·Neurology
9616240-2006-00341
FDA Adverse Event
Malfunction
·Product code FII·June 14, 2006
9616240-2006-00332
FDA Adverse Event
Other
·Product code FII·June 1, 2006