27 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ETHEREA
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Perflex Biosens
FDA UDI
PERFLEX LTD·07290110501556·Box of 6 Large cartridges 25mm diameter and 98m...
2430 BALLOON CONTROLLER
FDA UDI
HANS RUDOLPH, INC.·00874750008926·2430 INFL-4 BALLOON CNTRL 115V
T-Crystal cartridges Standard Pink
FDA UDI
PERFLEX LTD·07290110500153·Box of 6 identical cartridges sealed in aluminu...
T-Crystal cartridges Clear
FDA UDI
PERFLEX LTD·07290110500184·Box of 6 identical cartridges sealed in aluminu...
TLIF/PLIF Disc Prep
FDA UDI
Life Spine, Inc.·00190837086893·
T-Crystal cartridges Standard Pink
FDA UDI
PERFLEX LTD·07290110506056·5 identical cartridges sealed in a vacuum bag ;...
SOPRO595 INTRA ORAL CAMERA
FDA 510(k)
FDA Class 1
·Dental
HTO PLATING SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
PENCAN®
FDA Adverse Event
Injury
·B BRAUN MELSUNGEN AG·Product code BSP·May 6, 2025
ECHI GREENVILLE NC 2
FDA Adverse Event
Other
·SORIN GROUP USA, INC.·Product code DTZ·November 22, 2011
ECHI GREENVILLE NC 2
FDA Adverse Event
Other
·SORIN GROUP USA, INC.·Product code DTZ·November 30, 2011
ROBOTIC ARM INTERACTIVE ORTHOPEDIC SYSTEM-RIO
FDA Adverse Event
Malfunction
·MAKO SURGICAL·Product code OLO·April 25, 2014
ROBOTIC ARM INTERACTIVE ORTHOPEDIC SYSTEM-RIO
FDA Adverse Event
Malfunction
·MAKO SURGICAL·Product code NPJ·April 25, 2014
STONYBROOK HSP NY NY 1
FDA Adverse Event
Other
·SORIN GROUP USA, INC.·Product code OEZ·September 15, 2015
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·May 14, 2013
EPIC II CRITICAL CARE BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·May 25, 2011
CERAMTEC CERAMIC INS/SLEEVE TRIDENT F
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS CORK·Product code MEH·August 7, 2008
C21785 IT TREVISO
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA·Product code GEI·December 14, 2012
PENCAN®
FDA Adverse Event
Injury
·B BRAUN MELSUNGEN AG·Product code BSP·April 10, 2025