21 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Renaissance X System
FDA 510(k)
FDA Class 2
·Neurology
Temptation NOW® A1 8g Bulk
FDA UDI
DEN-MAT HOLDINGS, LLC·00359883006280·Crown and Bridge Temporary Resin
LACTOSORB SYSTEM
FDA UDI
BIOMET MICROFIXATION, INC·00841036067991·
Femoral Head
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215053536·
Signature Femoral Head
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215001766·
5.2MHZ PENCIL PROBE 10'
FDA UDI
PARKS MEDICAL ELECTRONICS, INC.·00816787020779·
Paxeon Femoral Head
FDA UDI
PAXEON RECONSTRUCTION LLC·08177570200269·Paxeon Head 40mm, CoCr Size S
OrthoMedFlex
FDA UDI
ORTHOMEDFLEX LLC·M7161111520410·Femoral Head, 40mm -4mm (S)
STINGRAY LP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DQY·March 26, 2025
COLLAGEN BONE HEALING PROTECTIVE SHEET
FDA 510(k)
FDA Class 2
·Orthopedic
AIXPLORER
FDA 510(k)
FDA Class 2
·Radiology
SIGNATURE Head - CoCr
FDA UDI
AMPLITUDE SAS·03701089520683·
STINGRAY? LP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DQY·May 29, 2026
PENUMBRA SYSTEM ACE 64 REPERFUSION CATHETER
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code NRY·July 17, 2015
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·October 8, 2014
XACT CAROTID STENT SYSTEM
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code NIM·July 7, 2011
BD ECLIPSE
FDA Adverse Event
Malfunction
·BD·Product code FMI·March 4, 2009
FLEXOR RADIAL ACCESS SET
FDA Adverse Event
Malfunction
·COOK INC·Product code DYB·December 12, 2017
FLEXOR RADIAL ACCESS SET
FDA Adverse Event
Malfunction
·COOK INC·Product code DYB·December 27, 2016
FLEXOR RADIAL ACCESS SET
FDA Adverse Event
Malfunction
·COOK INC·Product code DYB·March 10, 2017