28 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BIOMET MICROFIXATION STERNAL CLOSURE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
CoRoent
FDA UDI
Nuvasive, Inc.·00887517636461·CoRoent Ant TLIF PEEK, 12x11x30mm 12°
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772813827·GENUMEDI PRO SILVER SIZE II
MEDIANT
FDA UDI
INTELLIGENT IMPLANT SYSTEMS, LLC·00814033021266·Mediant Positioning Pins, Re-usable
N/A
FDA UDI
TETRA MEDICAL SUPPLY CORP.·00614138106147·TETRA-FOAM KNEE IMMOBILIZER, 20IN, REGULAR
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973714·
Integra® Jarit®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780466666·Integra® Jarit® French Eye Needle Holder, 7-1/4...
MYLABSEVEN, MYLABALPHA
FDA 510(k)
FDA Class 2
·Radiology
ALEUTIAN IBF SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
EVEREST® Spinal System
FDA UDI
VB Spine LLC·10888857550964·Trocar Size 200 mm
NV GXL LINER NEUTRAL, 32MM ID GROUP 1 CUPS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JDI·September 5, 2024
NV GXL LINER LIPPED 32MM ID, GROUP 1 CUPS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JDI·September 5, 2024
ALT HA S CLR EXT
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code MEH·November 14, 2023
M-SERIES
FDA UDI
Savaria Concord Lift·10688503000986·Patient lifter
M-SERIES
FDA UDI
Savaria Concord Lift·10688503000627·Patient lifter
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 20, 2013
RESTORE SENSOR
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·September 26, 2014
ASR ACETABULAR CUPS 52
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 1, 2011
NV GXL LINER NEUTRAL, 36MM ID, GROUP 2 CUPS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JDI·May 31, 2024
NV GXL LINER NEUTRAL, 32MM ID GROUP 1 CUPS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JDI·August 12, 2024