50 results
·
30ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
CREED Cannulated Screws
FDA 510(k)
FDA Class 2
·Orthopedic
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772777631·LUMBAMED BASIC DORSAL STAYS M SILVER I
Dornier MedTech
FDA UDI
Dornier MedTech GmbH·04049958001741·400 Micron Disposable Diode Laser Lightguide, 0...
Targeting Guide
FDA UDI
Treace Medical Concepts, Inc.·00810111223911·Guide Targeter
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776165543·PRONG VOLKMAN RETRACTOR SHARP
Integra® Jarit®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780372066·Integra® Jarit® Volkman Retractor, 9", USA Patt...
Ditron Dental
FDA UDI
DITRON DENTAL LTD·07290109285801·Short Implant Torque Driver Hex 2.42
EXACTECH, MODEL PMMA FEMORAL STEM CENTRALIZER
FDA 510(k)
FDA Class 2
·Orthopedic
MFCD 118
FDA 510(k)
FDA Class 2
·Radiology
MPACT ACETABULAR SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·October 31, 2025
MPACT EXTENSION
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code MEH·April 2, 2026
MPACT ACETABULAR SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·July 18, 2025
MECTACER BIOLOX DELTA FEMORAL BALL HEAD
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·December 19, 2024
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·September 25, 2020
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·September 14, 2022
T:SLIM G5 SYSTEM
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code OYC·April 10, 2019
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·January 20, 2023
BTA3D COMBINATION MODULE LEFT - 200291
FDA Adverse Event
Malfunction
·BIOMERIEUX INC.·Product code MDB·November 28, 2022
BACT/ALERT® I NST
FDA Adverse Event
Malfunction
·BIOMÉRIEUX, INC.·Product code MDB·April 20, 2022
BACT/ALERT 3D COMBINATION
FDA Adverse Event
Malfunction
·BIOMERIEUX INC.·Product code MDB·December 22, 2020