12 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SORRENTO BONE GRAFT SUBSTITUTE
FDA 510(k)
FDA Class 2
·Orthopedic
Novo Surgical
FDA UDI
NOVO SURGICAL, INC.·G586G1414290·operating scissors, blunt/blunt, curved, 7 1/4"...
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515019300·Adson Artery Forceps,orig curved, 8 1/4"
K2M General Instruments
FDA UDI
VB Spine LLC·10888857581241·Split Tube Retractor Ø16x110 mm
ECO SUPERGEL
FDA 510(k)
FDA Class 2
·Radiology
SENSITITRE (R) HP MIC SUSCEPTIBILITY PLATE WITH CEFAROLINE (0.004-8UG/ML) AND THE SENSITITRE (R) 18-24 HOUR MIC SUSCE...
FDA 510(k)
FDA Class 2
·Microbiology
GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 6/13 MM R
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·June 4, 2020
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·April 29, 2026
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·November 12, 2012
OT VERIO SYNC METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 4, 2014
EON MINI
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 24, 2013
GOBED II
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·June 1, 2011