29 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ITERO SOFTWARE
FDA 510(k)
FDA Class 2
·Dental
Pilot Spinal System
FDA UDI
Life Spine, Inc.·00190837051303·Pilot 7mm Wrench
Tasso+ Convenience Kit
FDA UDI
Tasso Inc.·00860006434526·Tasso+ allows self-collection of a capillary bl...
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690128960·Femoral Augment, Notched Posterior, Size 1, 10mm
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690196754·NOTCHED POSTERIOR AUGMENT TRIAL REVISION FEMUR ...
LIF Access
FDA UDI
ALPHATEC SPINE, INC.·00190376205700·LIF-PTP Lateral Bolster, Round
Life Instruments
FDA UDI
Life Instrument Corporation·M93071311010C0·Custom 11.5" Micro Curette #1 STR
RAICHEM ASSAYED CONTROL SERUM LEVEL 1 & 2
FDA 510(k)
FDA Class 1
·Clinical Chemistry
MINI-TONG
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ONE TOUCH PROFILE
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·November 27, 2001
SURESTEP
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code CGA·March 11, 1999
DIGITAL RADIOGRAPHY CXDI
FDA Adverse Event
Malfunction
·CANON, INC.·Product code MQB·December 22, 2019
DIGITAL RADIOGRAPHY CXDI
FDA Adverse Event
Malfunction
·CANON, INC.·Product code MQB·December 22, 2019
DIGITAL RADIOGRAPHY CXDI
FDA Adverse Event
Malfunction
·CANON, INC.·Product code MQB·December 22, 2019
ASTRAL 150 - FUKUDA
FDA Adverse Event
Malfunction
·RESMED LTD·Product code NOU·December 7, 2016
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 1, 2014
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 16, 2011
CHARGING SYSTEM
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 23, 2013
MITRACLIP® SYSTEM CLIP DELIVERY SYSTEM
FDA Adverse Event
Death
·ABBOTT MEDICAL·Product code NKM·October 11, 2022
MITRACLIP® SYSTEM CLIP DELIVERY SYSTEM
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code NKM·October 11, 2022