9 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ATRAUMATIC VASCULAR CLAMPS, MODEL #'S 22-XXXX, 23-XXXX, 03-60XX, 25-XXXX MICRO VASCULAR CLAMPS MODEL # 75-0XXX, ATRAUMAT
FDA 510(k)
FDA Class 2
·Cardiovascular
N/A
FDA UDI
Key Scientific Products Incorporated·00850041798028·PEP REAGENT
N/A
FDA UDI
Key Scientific Products Incorporated·00850041798042·Pep ReagentT
TempSure System
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
HERAEUS LASERSONICS ND:YAG LASER, MODEL 4900
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
6.0MMTI PANGEA (TM) POLYAXIAL
FDA Adverse Event
Injury
·SYNTHES BRANDYWINE·Product code NKB·February 26, 2013
TOTALCARE BARIATRIC
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·January 13, 2011
530G INSULIN PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·August 5, 2014
STA-Flex SUBTALAR SCREW, 11 mm x 17 mm, REF 982365, Sterile, Biomet Sports Medicine, 56 East Bell Drive, Warsaw, IN. Used to reduce excessive rearfoot pronation by blocking forward and downward displacement of the Talus, resulting in improved rearfoot alignment and foot function.
FDA Recall
Terminated
·Biomet, Inc.·Product code HWC·January 21, 2011