22 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SLIC SCREW REPAIR SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
OsteoMed
FDA UDI
OSTEOMED LLC·00845694002394·1.6mm x 8mm AUTO-DRIVE Screw
Sklar®
FDA UDI
SKLAR CORPORATION·10649111167096·STILLE PLASTER SHEAR 7.75"
MicroSelectron Digital
FDA UDI
Nucletron B.V.·08717213026155·microSelectron Transfer Tube for 4F Flexibles (26)
OsteoMed
FDA UDI
OSTEOMED LLC·00845694031042·1.6mm x 8mm Auto-Drive Screw, Sterile
Specials
FDA UDI
Seaspine Orthopedics Corporation·10889981319731·16x14x08 Trial Rasp, w/ Depth Stop
OsteoMed
FDA UDI
OSTEOMED LLC·00845694054539·1.6mm x 8mm Auto-Drive Screw Sterile Qty 10
OsteoMed
FDA UDI
OSTEOMED LLC·00845694044035·1.6mm x 8mm AUTO-DRIVE Screw
MODEL 235GE-64; MULTI PURPOSE FLEX ARRAY COIL
FDA 510(k)
FDA Class 2
·Radiology
BIOMET 3I PATIENT SPECIFIC DENTAL ABUTMENTS-ENCODE ABUTMENTS
FDA 510(k)
FDA Class 2
·Dental
Ascendant
FDA UDI
Choice Spine, LP·10885862260802·
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FKX·May 14, 2013
SOFTCLIX ® LANCET DEVICE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FMK·June 2, 2011
EAGLE 4000
FDA Adverse Event
Malfunction
·GE HEALTHCARE·Product code LOS·August 13, 2008
RGDLOOP ADJUSTABLE STND
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SÃ RL·Product code MBI·April 6, 2020
RGDLOOP ADJUSTABLE STND
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SÃ RL·Product code MBI·March 2, 2020
RGDLOOP ADJUSTABLE STND
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SÃ RL·Product code MBI·January 23, 2020
RGDLOOP ADJUSTABLE STND
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SÃ RL·Product code MBI·December 18, 2019
RGDLOOP ADJUSTABLE STND
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SÃ RL·Product code MBI·December 19, 2019
INLIVEN CRT-P, Model Numbers: a) V284 b) V285 c) W274 d) W275 (added 7/15/2021)
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·July 21, 2021