28 results
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32ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CAPENERGY - C100, C200, C300, C400, C50
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772813827·GENUMEDI PRO SILVER SIZE II
Edge™ Diamond ND010-4F Needle
FDA UDI
CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172002592·Diamond dental bur, reusable
Mueller Nasal Sponges
FDA UDI
Mueller Sports Medicine, Inc.·00074676191225·NASAL SPONGES, 5 PACK
LinkBio Instrument
FDA UDI
Link Bio Corp·00810022402993·Impactor Plate, Tibial Cone Small
Hysteroscopy sheath
FDA UDI
SOPRO-COMEG GmbH·04059082032504·
Hysteroscopy sheath
FDA UDI
SOPRO-COMEG GmbH·04059082006055·
EXACTECH
FDA Adverse Event
Malfunction
·EXACTECH, INC.·Product code LHX·April 11, 2022
SURGICAL TISSUE MANAGEMENT SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
WEDGELOC 180X STANDARD SUTURE ANCHOR WITH OPTI FIBER SUTURES,MODEL 1000-01 TAB VARYING DIAMETERS,
FDA 510(k)
FDA Class 2
·Orthopedic
EXACTECH
FDA Adverse Event
Malfunction
·EXACTECH, INC.·Product code LXH·March 28, 2022
EXACTECH
FDA Adverse Event
Malfunction
·EXACTECH, INC.·Product code LXH·March 29, 2022
EXACTECH
FDA Adverse Event
Malfunction
·EXACTECH, INC.·Product code LXH·March 30, 2022
EXACTECH
FDA Adverse Event
Malfunction
·EXACTECH, INC.·Product code LXH·March 30, 2022
EXACTECH
FDA Adverse Event
Malfunction
·EXACTECH, INC.·Product code LXH·March 30, 2022
EXACTECH
FDA Adverse Event
Malfunction
·EXACTECH, INC.·Product code LXH·March 29, 2022
MINICAP TRANSFER SET
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·June 26, 2013
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 19, 2011
PROLIEVE TEMPERATURE MONITOR
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code MEQ·September 26, 2008
SCREW REMOVAL TOOL (STAINLESS STEEL)
FDA Adverse Event
Injury
·ALPHATEC SPINE INC·Product code LXH·December 10, 2014