18 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Sterile Dilator
FDA 510(k)
FDA Class 2
·Cardiovascular
NA
FDA UDI
Stryker GmbH·07613154481958·Drill, WL 26.5mm, Stryker-Shaft
Sklar
FDA UDI
SKLAR CORPORATION·10649111452079·BROWN RESANO DRESS FORCEPS 8 INCHES
SP-FIX SPINOUS PROCESS FIXATION PLATE
FDA 510(k)
FDA Class 2
·Orthopedic
CUTERA MULTIMODAL CELLULITE PRODUCT (CMMCD)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
N/A
FDA UDI
Exactech, Inc.·10885862659897·Trial, Monobloc Revision Stem
NA
FDA UDI
Exactech, Inc.·10885862282811·TRIAL, MONOBLOC REVISION STEM, 19x195mm
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·January 23, 2023
PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAW·June 13, 2018
FINELINE II
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code DTB·April 10, 2017
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 4, 2011
ACCENT DR RF
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·January 13, 2014
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 20, 2013
UNKNOWN PROGRIP MESH PRODUCT
FDA Adverse Event
Injury
·SOFRADIM PRODUCTION·Product code FTL·March 20, 2015
FLEXTEND
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVN·July 20, 2011
UNKNOWN PROGRIP MESH PRODUCT
FDA Adverse Event
Injury
·SOFRADIM PRODUCTION·Product code FTL·March 11, 2015
ENDOPATH*MULTIFEED STAPLER
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·August 16, 2019
PROLENE POLYPROPYLENE MESH UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code FTL·August 22, 2019