67 results
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36ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Kalitec Universal Instruments
FDA UDI
Kalitec Direct LLC·B07301K1103500·Tray, Base, 3.5", Arcamed
KNEEHAB XP
FDA 510(k)
FDA Class 2
·Neurology
PIVOX™ Oblique Lateral Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169601260·SPACER 2110350 OLIF25 20MM 0 DEG 12X50
TRESTLE LUXE
FDA UDI
ALPHATEC SPINE, INC.·00190376215006·TRESTLE LUXE II, ACP, 3-LEVEL, 50
Humeris Shoulder
FDA UDI
FX SOLUTIONS·03701037306772·STOP DRILL BIT Ø5.0 mm L.150 mm/AO
5.0MM VARIABLE ANGLE LOCKNG SCREW/SLF-TPNG/STRDRV/65MM
FDA Adverse Event
Injury
·SYNTHES MEZZOVICO·Product code JDP·August 28, 2015
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K1100500·Caddie, 4.75mm Screws
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·January 26, 2015
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·March 2, 2015
IMPLANT, FIXATION DEVICE CONDYLAR PLATE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code JDP·February 23, 2017
STA -CALIBRATOR HBPM/LMWH KIT
FDA 510(k)
FDA Class 2
·Hematology
HOVEROUND TEKNIQUE GT POWER WHEELCHAIR, MODEL# TEKNIQUE GT
FDA 510(k)
FDA Class 2
·Physical Medicine
T:SLIM G5 SYSTEM
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code OYC·April 10, 2020
T:SLIM X2 INSULIN PUMP WITH INTEROPERABLE TECHNOLOGY (WITH T:CONNECT MOBILE APP)
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·March 11, 2024
TRULIANT TIB IMP PS INSERT SZ 5 11MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·April 10, 2024
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·May 7, 2025
TRULIANT TIB IMP PS INSERT SZ 5 11MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·May 19, 2023
OT VERIO TEST STRIPS
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 13, 2013
CORE IMPACTION DRILL
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS-KALAMAZOO·Product code ERL·September 23, 2014
SECURE 3 MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·May 20, 2011