23 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EDGE CO2 LASER SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Aira
FDA UDI
AIRA, LLC·00810194400704·2.25" x 4" - Paper/Blue Film Self-Sealing Steri...
Bleep Halos
FDA UDI
BLEEP, LLC·00850003157115·
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450555774·
HS Diam. Burr, Ø4.0x125, 80k
FDA UDI
Bien-Air Surgery SA·17630055507317·
Nitanium® Super Elastic Archwires
FDA UDI
Ortho Organizers, Inc.·00190707088088·.016x.022 Upper Nitanium® Dimple Reverse Curve ...
House Brand Dentistry
FDA UDI
Frontier Dental Supply Inc·00810132809477·HSB - 2.25" x 4" - Paper/Blue Film Self-Sealing...
N/A
FDA UDI
Doppkon GmbH & Co. KG·04262494461583·Cup Forceps Straight Jaw
D 5.0mm, WL 180mm
NEUROPACK MICRO, MODEL MED-9100A SERIES
FDA 510(k)
FDA Class 2
·Physical Medicine
LATERAL PIVOT INSERT
FDA 510(k)
FDA Class 2
·Orthopedic
LINEAR ST
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·November 7, 2023
G7 FINNED 4 HOLE SHELL 54F
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·November 28, 2017
TANDEM T:SLIM INSULIN DELIVERY SYSTEM
FDA Adverse Event
Injury
·TANDEM DIABETES CARE·Product code LZG·March 28, 2017
HEARTMATE II LVAS
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·May 8, 2013
GRANUFLO
FDA Adverse Event
Death
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·September 17, 2014
TERUMO CDI 500 BLOOD PARAMETER MONITOR
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEM CORP.·Product code DRY·May 13, 2011
TAPERLOC COMPETE PRIMARY FEMORAL POROUS COSTED STEM 16X 152MM HIGH OFFSET TYPE 1
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·July 12, 2017
UNKNOWN HEAD
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LZO·November 28, 2017
UNKNOWN LINER
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PBI·November 28, 2017
UNKNOWN TAPER
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LZO·November 28, 2017