15 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HF-Etchant Hydrofluoric Acid Etching Gel
FDA 510(k)
FDA Class 2
·Dental
Artman Instruments
FDA UDI
Wise Linkers, LLC·D1272425301·William Periodontal Probes Probing Pocket Depth...
NA
FDA UDI
SYNTHES (U.S.A.) LP·10886982168733·WRIST FUSION PLATE 9 HOLES/STRAIGHT
CERTAIN® TITANIUM LARGE HEXED SCREW
FDA Adverse Event
Malfunction
·BIOMET 3I·Product code DZE·March 25, 2022
CERTAIN TITANIUM LARGE HEXED SCREW
FDA Adverse Event
Malfunction
·BIOMET 3I·Product code DZE·May 20, 2021
CERTAIN TITANIUM LARGE HEXED SCREW
FDA Adverse Event
Malfunction
·BIOMET 3I·Product code DZE·May 20, 2021
CERTAIN® TITANIUM LARGE HEXED SCREW
FDA Adverse Event
Malfunction
·BIOMET 3I·Product code DZE·March 25, 2022
CERTAIN® TITANIUM LARGE HEXED SCREW
FDA Adverse Event
Malfunction
·BIOMET 3I·Product code DZE·March 25, 2022
CONSERVE PLUS HA ACETABULAR SHELLS
FDA 510(k)
FDA Class 3
·Orthopedic
Partial Knee Application (PKA)
FDA 510(k)
FDA Class 2
·Neurology
ALARIS INFUSION SYSTEM
FDA Adverse Event
Other
·CARDINAL HEALTH ALARIS PRODUCTS·Product code FRN·November 21, 2008
DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·September 10, 2011
M2A-38 CUP NON FLARED SIZE 56MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·July 23, 2013
HANDPIECE MICS
FDA Adverse Event
Malfunction
·MAKO SURGICAL CORP.·Product code OLO·May 23, 2018
Direct Drive Clip Applier CA090, indicated for ligation of tubular structures or vessels in laparoscopic and general surgical procedures. Distributed individually and in kits.
FDA Enforcement
Class II
·Terminated·Applied Medical Resources Corp·May 18, 2016