16 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ENDOLIGHT LED 1.1 ENDOLIGHTLED 1.2
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
NOVO Health Services, LLC
FDA UDI
NOVO HEALTH SERVICES, LLC·00812564032348·Cover, Mayo Stand w/o Twl
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450414118·
UniTip Catheter
FDA UDI
Unisensor AG·07640172973875·
GRIPTION
FDA UDI
DEPUY (IRELAND)·10603295381358·GRIPTION TF SCREW 5.5mm x 24mm
MiniSPC Button
FDA UDI
APPLIED MEDICAL TECHNOLOGY, INC.·00842071152222·12F x 1.7cm MiniSPC Low Profile Suprapubic Cath...
UniTip Catheter
FDA UDI
Unisensor AG·07640172973790·
STRAUMANN TIBRUSH
FDA 510(k)
FDA Class 2
·Dental
DORNIER DIODE LASER FAMILY, INCLUDING MEDILAS D FIBERTOM, MEDILAS D SKINPULSE & MEDILAS D SKINPULSE S LASER SYSTEMS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ANGEL SYSTEM WITH ASPIRATION KIT W/ ACDA
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code ORG·March 5, 2019
ARTHREX ANGEL SYSTEM WITH ASPIRATION KIT
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code ORG·May 1, 2019
HYPERFORM OCCLUSION BALLOON SYSTEM
FDA Adverse Event
Malfunction
·EV3 NEUROVASCULAR·Product code MJN·May 21, 2013
FLOGARD
FDA Adverse Event
Malfunction
·SHARP CORPORATION OSAKA JAPAN·Product code FRN·September 26, 2014
OSCILLATING AND SAGITTAL BLADE
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS CORK·Product code GFA·May 19, 2011
THINFLAP SYSTEM CROSS-DRIVE, SELF-DRILLING SCREW 1.5X4MM
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code GWO·April 16, 2018
MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·September 27, 2024