23 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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UNIVERSAL PASTE STAINS AND GLAZE
FDA 510(k)
FDA Class 2
·Dental
EVONOS
FDA UDI
Gyrus ACMI, LLC·00821925014015·MONTGOMERY PTERYGOMAXILLARY ELEV, S
ALEUTIAN Interbody Systems
FDA UDI
VB Spine LLC·10888857560734·Disc Spreader Size 8 mm
OTIS -C PLUS
FDA 510(k)
FDA Class 2
·Orthopedic
PERFECT SAFETY SYRINGE
FDA 510(k)
FDA Class 2
·General Hospital
UniTip Catheter
FDA UDI
Unisensor AG·07640172971345·
M-SERIES
FDA UDI
Savaria Concord Lift·10688503001655·Patient lifter
UniTip Catheter
FDA UDI
Unisensor AG·07640172973639·
UniTip Catheter
FDA UDI
Unisensor AG·07640172971338·
UniTip Catheter
FDA UDI
Unisensor AG·07640172973219·
MAGEC SPINAL BRACING AND DISTRACTION SYSTEM
FDA Adverse Event
Malfunction
·NUVASIVE SPECIALIZED ORTHOPEDICS, INC.·Product code PGN·April 14, 2021
AMISTEM H, HA COATED STEM SIZE 6 STD
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·June 9, 2017
MOTORIZED 3-WHEELED VEHICLE FOR OUTSIDE TRANSPORT
FDA Adverse Event
C.T.M. HOMECARE PRODUCT, INC·Product code INI·May 24, 2013
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·September 30, 2014
FLANGE FIXTURE AND ABUTMENT
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·June 16, 2011
VENTED HUMIDIFICATION CHAMBER
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·December 18, 2013
ADULT DUAL HEATED BREATHING CIRCUIT
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTT·November 12, 2013
VENTED HUMIDIFICATION CHAMBER
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTT·December 22, 2013
ESTEEM
FDA Adverse Event
Injury
·ENVOY MEDICAL CORPORATION·Product code OAF·August 29, 2019
13 CM TRICUT BLADE
FDA Adverse Event
Malfunction
·MEDTRONIC ENT (JACKSONVILLE)·Product code HAW·July 23, 2015