18 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SeaSpine Cambria System
FDA 510(k)
FDA Class 2
·Orthopedic
K-Wire and Steinmann Pin Dispensers
FDA UDI
KEY SURGICAL, INC.·00849771046370·K-Wire and Steinmann Pin Dispensers, Dispensing...
OSE
FDA UDI
ORTHODONTIC SUPPLY & EQUIPMENT COMPANY INC·00810042121010·Round Buccal Tubing - .045
STOCKERT S5 SYSTEM AND GAS BLENDER AND SORIN C5 SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
SYNTHES CHRONOS COMPOSITE
FDA 510(k)
FDA Class 2
·Orthopedic
TRULIANT PS CEM FEM PS CEM RIGHT SZ 4.5
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·August 15, 2024
BD INTIMA-II Y 20GAX1.16IN PRN/EC SLM
FDA Adverse Event
Malfunction
·BD SUZHOU (MDS)·Product code FOZ·February 25, 2025
ELECTRONIC GAS BLENDER
FDA Adverse Event
Malfunction
·LIVANOVA DEUTSCHLAND·Product code DTX·November 19, 2025
STOCKERT S3 GAS BLENDER
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·December 22, 2014
8.0MM DRILL BIT FOR DHS/DCS TRIPLE REAMER
FDA Adverse Event
Malfunction
·SYNTHES HAGENDORF·Product code HTW·October 14, 2014
PROSTAR XL SUTURE-MEDIATED CLOSURE
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·June 14, 2013
5.0MM LOCKING SCREW
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HWC·July 8, 2011
S3 GAS BLENDER SYSTEM
FDA Adverse Event
Malfunction
·LIVANOVA DEUTSCHLAND·Product code DTX·October 16, 2017
S3 GAS BLENDER SYSTEM
FDA Adverse Event
Malfunction
·LIVANOVA DEUTSCHLAND·Product code DTX·October 16, 2017
S3 ELECTRONIC GAS BLENDER
FDA Adverse Event
Malfunction
·LIVANOVA DEUTSCHLAND·Product code DTX·December 19, 2024
SORIN S3 GAS BLENDER
FDA Adverse Event
Malfunction
·SORIN GROUP DEUTSCHLAND·Product code DTX·February 25, 2015
BD INTIMA-II Y 20GAX1.16IN PRN/EC SLM
FDA Adverse Event
Malfunction
·BD SUZHOU (MDS)·Product code FOZ·March 19, 2025
TRU CC FEMORAL SIZE 1 LEFT
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·October 15, 2025