24 results
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52ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772814671·GENUMEDI SILVER SIZE IV
IMPACT LIP-LOC HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304211827·
DD tempMED
FDA UDI
Dental Direkt GmbH·EDDIK112201·DD tempMED are pre-colored dental milling blank...
Universal Neuro 2, Universal Neuro 3
FDA UDI
Stryker Leibinger GmbH & Co. KG·04546540543011·DRILL, WL 4MM, DENTAL SHAFT
DENALI
FDA UDI
ORTHODONTIC SUPPLY & EQUIPMENT COMPANY INC·00810042120273·Curved Bracket Tweezer
T-Crystal cartridges Standard Pink
FDA UDI
PERFLEX LTD·07290110506346·5 identical cartridges sealed in a vacuum bag ;...
K2M General Instruments
FDA UDI
VB Spine LLC·10888857529885·Replaceable Tip
BRAINLAB TRAUMA
FDA 510(k)
FDA Class 2
·Neurology
CELL-DYN 22 PLUS CALIBRATOR
FDA 510(k)
FDA Class 2
·Hematology
CHOICE SPINE STARFIRE PEDICLE SCREW SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·February 28, 2022
LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·May 3, 2013
ROD TO ROD COUPLING HOFFMANN II MICRO 3/3MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS SELZACH·Product code KTT·April 29, 2011
DCA 2000 SYSTEM FOR HBA1C
FDA Adverse Event
Other
·BAYER CORP.·Product code LCP·August 6, 2008
NSK
FDA Adverse Event
Malfunction
·NAKANISHI INC.·Product code EFB·December 6, 2018
NSK
FDA Adverse Event
Malfunction
·NAKANISHI INC.·Product code EFB·December 6, 2018
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·August 8, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·May 2, 2022
NSK
FDA Adverse Event
Injury
·NAKANISHI INC.·Product code EFB·February 11, 2020
IPI Ventilator Circuit with 2 Water Traps, product reorder no. 6066; SIngle Patient Use Only; Manufactured by IPI Medical Products, 3217 N. Kilpatrick St., Chicago, IL 60641
FDA Recall
Terminated
·Medex Inc·Product code BZO·July 12, 2004