9 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SILKPRO Titanium Diode Laser System SILKPRO-S20S-TWC
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
TriVerse Asymmetric Patella Trial
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215098346·
CD HORIZON SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
TRANSCURE, MODEL 2910
FDA 510(k)
FDA Class 2
·Dental
TRILOGY ACETABULAR SHELL WITHOUT HOLES
FDA Adverse Event
Malfunction
·ZIMMER,·Product code LPH·August 10, 2011
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE REHABILITATION EQUIP·Product code ITI·November 4, 2014
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·July 12, 2013
CD HORIZON® SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·November 25, 2024
syngo.via RT Image Suite with syngo.via VB30, VB40, VB50 and VB60- Intended for Radiation Therapy Treatment Material Number: 10496180
FDA Enforcement
Class II
·Ongoing·Siemens Medical Solutions USA, Inc·September 22, 2021