22 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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L100 Go System
FDA 510(k)
FDA Class 2
·Neurology
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772777648·LUMBAMED BASIC DORSAL STAYS M SILVER II
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772777594·LUMBAMED BASIC DORSAL STAY WM SILVER II
FORCEPS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896060708·FORCEPS EXTRA LONG STRAIGHT TUNGSTEN CARBIDE DU...
OsteoMed
FDA UDI
OSTEOMED LLC·00845694034463·BLUE METAL SCREWDRIVER BODY
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112557·BARRON VACUUM TREPHINE 9.0MM
SCANLAN®
FDA UDI
SCANLAN INTERNATIONAL INC·00846159007640·Dennis Anastomosis Clamp
BALANCE MICROPLASTY BROACH
FDA UDI
Biomet Orthopedics, LLC·00880304459281·
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306836466·Joseph Nasal Knife, Blunt, Curved, 16cm
Foot and Ankle System
FDA 510(k)
FDA Class 2
·Orthopedic
BOHN FEMORAL COMPONENT
FDA 510(k)
FDA Class 2
·Orthopedic
T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code OZO·May 29, 2020
PUMP MMT-1780KPK 670G PATHWAY BLACK MG
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·April 23, 2019
BLUE METAL SCREWDRIVER BODY
FDA Adverse Event
Malfunction
·OSTEOMED, LLC·Product code HXX·July 28, 2025
ANIMAS VIBE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·October 24, 2014
IDENTITY ADX DR
FDA Adverse Event
Death
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWP·August 11, 2011
PROGRAMMING SOFTWARE
FDA Adverse Event
Malfunction
·CYBERONICS·Product code LYJ·July 1, 2013
Barron Radial Vacuum Trephine (1) Complete Trephine Set 9.0mm Dia. Ref. K20-2062 Lot 122336 Opthalmic
FDA Recall
Terminated
·Surgical Instrument Service And Savings, Inc.·Product code HRH·May 3, 2013
Barron Radial Vacuum Trephine (1) Complete Trephine Set 9.0mm Dia. Ref. K20-2062 Lot 122336 Opthalmic
FDA Enforcement
Class II
·Terminated·Surgical Instrument Service And Savings, Inc.·July 10, 2013
TRUEMETRIX
FDA Adverse Event
Malfunction
·TRIVIDIA HEALTH, INC.·Product code NBW·March 9, 2017