37 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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ORTHOLOC® 3Di Foot Plating Reconstruction System
FDA 510(k)
FDA Class 2
·Orthopedic
APEX Revision Knee
FDA UDI
Omni Life Science, Inc.·00841690124726·Modular Offset Stem 9mm x 75mm x 4mm
INTELLISPHERE EVENT MANAGMENT SYSTEM REL. 10.00
FDA 510(k)
FDA Class 2
·Cardiovascular
WARMING LIQUID PERSONAL LUBRICANT
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
NexGen
FDA UDI
Zimmer, Inc.·00889024568648·
NexGen
FDA UDI
Zimmer, Inc.·00889024568600·
NexGen
FDA UDI
Zimmer, Inc.·00889024568594·
NexGen
FDA UDI
Zimmer, Inc.·00889024568679·
NexGen
FDA UDI
Zimmer, Inc.·00889024568631·
NexGen
FDA UDI
Zimmer, Inc.·00889024568655·
NexGen
FDA UDI
Zimmer, Inc.·00889024568587·
NexGen
FDA UDI
Zimmer, Inc.·00889024568624·
NexGen
FDA UDI
Zimmer, Inc.·00889024568662·
NexGen
FDA UDI
Zimmer, Inc.·00889024568617·
BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B LABORATORY KIT
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·March 3, 2026
PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE
FDA Adverse Event
Injury
·MEDTRONIC MILACA, INC.·Product code LWP·June 8, 2013
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 7, 2011
HOMECHOICE PRO
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·October 8, 2014
UNKNOWN PLATE
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code HRS·April 21, 2026
UNKNOWN PLATE
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code HRS·April 21, 2026