39 results
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31ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Arcus Staple System
FDA 510(k)
FDA Class 2
·Orthopedic
AGC TRADITION KNEE SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304241350·
ProLift
FDA UDI
Life Spine, Inc.·00190837117320·
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690192374·Apex Revision Knee Reamer - Zimmer 16mm
OsteoMed
FDA UDI
OSTEOMED LLC·00845694046831·PrimaLIF LLIF PEEK Implant, 11mm X 18mm X 60mm,...
Pro Lift Instruments
FDA UDI
Life Spine, Inc.·00190837031152·
CMF SYSTEM
FDA UDI
BIOMET MICROFIXATION, INC·00841036032401·
MANIPUSEAL
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
ROCHE ORAL FLUID COCAINE
FDA 510(k)
FDA Class 2
·Clinical Toxicology
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·October 5, 2023
NY-STA BLACK 2/0 18" (45CM) DS24 VPL
FDA Adverse Event
Malfunction
·B. BRAUN SURGICAL, S.A.·Product code GAR·May 5, 2026
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·August 18, 2023
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2013
LORENZ STERNAL CLOSURE SYSTEM WITH MODULAR SCREW
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code HRS·October 8, 2014
AUGMENTED INSERT
FDA Adverse Event
Injury
·DEPUY-CORK, A DIVISION OF DEPUY ORTHOPAEDICS·Product code KWA·June 30, 2011
SUPRAMID BLACK 3/0 (2) 45CM DS19
FDA Adverse Event
Malfunction
·B. BRAUN SURGICAL, S.A.·Product code GAR·June 13, 2022
DAFILON 3/0 (2) 100M
FDA Adverse Event
Malfunction
·B. BRAUN SURGICAL, S.A.·Product code GAR·December 27, 2023
INTELLIS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·August 14, 2025
TRUE METRIX GO
FDA Adverse Event
Malfunction
·TRIVIDIA HEALTH INC·Product code NBW·January 11, 2024
SKIN SUTURE PACK DAFILON
FDA Adverse Event
Malfunction
·B. BRAUN SURGICAL, S.A.·Product code GAR·July 18, 2024