30 results
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23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DR180-II
FDA 510(k)
FDA Class 2
·Cardiovascular
Custom Procedure Kit
FDA UDI
MEDIVATORS INC.·40677964011502·Endo Carry-On Procedure Kit
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040044308·Knife Goldman Fox DE #11
artVeneer life
FDA UDI
Merz Dental GmbH·D7092001288·artVeneer life lower anteriors, UBL, B4
ADVANCE®
FDA UDI
Microport Orthopedics Inc.·M684K00012881·
Vista
FDA UDI
Modus Medical Devices Inc·G34350012881·40 mm PET jar with lid - box of 100
ULTRASIM CT SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
REICHERT CT200 CONTACT TONOMETER
FDA 510(k)
FDA Class 2
·Ophthalmic
EVOLUTION MP CS INSERT SIZE 7 STANDARD 10MM LEFT
FDA Adverse Event
Injury
·MICROPORT ORTHOPEDICS INC.·Product code HRY·March 16, 2020
EVOLUTION MP CS INSERT SIZE 8 STANDARD 12MM LEFT
FDA Adverse Event
Malfunction
·MICROPORT ORTHOPEDICS INC.·Product code HRY·April 13, 2020
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·May 23, 2026
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·February 22, 2026
UNIVERSAL SLING BAR
FDA Adverse Event
Other
·LIKO AB·Product code FSA·February 28, 2013
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·February 24, 2011
LIFEVEST WCD 3000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·February 19, 2008
SYRINGE 20ML LL 120/PKG
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·June 4, 2020
ADVANCE® ONLAY ALL-POLY PATELLA 32MM TRI-PEG
FDA Adverse Event
Injury
·MICROPORT ORTHOPEDICS INC.·Product code JWH·November 1, 2022
EVOLUTION® NITRX? TIB KEELED
FDA Adverse Event
Injury
·MICROPORT ORTHOPEDICS INC.·Product code JWH·November 7, 2022
EVOLUTION® NITRX? TIB KEELED
FDA Adverse Event
Injury
·MICROPORT ORTHOPEDICS INC.·Product code JWH·November 7, 2022
EVOLUTION® NITRX? FEM CS/CR NONPOR TINBN COATED SI
FDA Adverse Event
Injury
·MICROPORT ORTHOPEDICS INC.·Product code JWH·December 14, 2022