641 results
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31ms
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Sources: EU EUDAMED, US FDA
INFUSE BONE GRAFT/LT-CAGE
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code OJZ·December 22, 2015
Stryker Biotech OP-1 Putty (OP-1, BMP-7, bone morphogenetic protein) "Catalog numbers: 300-50, 300-55 OP-1 Putty is authorized by Federal law for use as an alternative to autograft in compromised patients requiring revision posterolateral (intertransverse) lumbar spinal fusion, for whom autologous bone and bone marrow harvest are not feasible or are not expected to promote fusion. Examples of compromising factors include osteoporosis, smoking and diabetes.
FDA Recall
Terminated
·Stryker Biotech·Product code OJZ·October 25, 2010
Filler, Recombinant Human Bone Morphogenetic Protein, Collagen Scaffold, Osteoinduction - Hde
FDA classification
Filler, Recombinant Human Bone Morphogenetic Protein, Collagen Scaffold, Osteoinduction - Hde
OJ-1 ENDODONIC ROOT CANAL FILE HOLDER
FDA 510(k)
FDA Class 1
·Dental
MJZ
FDA UDI
Yangzhou Yichuan Plastic Technology Co., Ltd.·06975808920017·
OTZ Partners, LLC
FDA registration
OTZ Partners, LLC·3 products·🇺🇸 United States
EYE OJO CORP.
FDA registration
EYE OJO CORP.·8 products·🇺🇸 United States
OMZ-100
FDA UDI
GTG Wellness Co., Ltd.·08809520341141·
OMZ-100
FDA UDI
GTG Wellness Co., Ltd.·08809520341134·
OLZ-200
FDA UDI
GTG Wellness Co., Ltd.·08809520341103·
OMZ-100
FDA UDI
GTG Wellness Co., Ltd.·08809520341165·
OLZ-200
FDA UDI
GTG Wellness Co., Ltd.·08809520341110·
ÖZ AKYEL MEDİKAL A.Ş.
Manufacturer
🇹🇷 Türkiye
Custom Healthcare Systems Inc.
FDA UDI
Manus Medical, LLC·00811870032110·
ZOLL-DENTAL
FDA UDI
Zoll-Dental·00840105207603·CJZ
NA
FDA UDI
MAR COR PURIFICATION, INC.·00817492021815·Ozone System
Hyper Tough
FDA UDI
Eye Ojo Corp.·00666197824883·
OZARK TRAIL
FDA UDI
Eye Ojo Corp.·00666197775345·
Hyper Tough
FDA UDI
Eye Ojo Corp.·00666197824203·
Hyper Tough
FDA UDI
Eye Ojo Corp.·00666197824302·