22 results
·
43ms
·
Sources: EU EUDAMED, US FDA
NES Reprocessed RF Stylet (RFS)
FDA registration
NORTHEAST SCIENTIFIC, INC.·2 products·🇺🇸 United States
NES Reprocessed RF Stylet (RFS)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
FDA classification
FDA Class 2
·Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772814770·GENUMEDI EXTRA WIDE SILVER SIZE IV
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526550193·GENUMEDI PT KNEE SUP SILVER R EW IV
CENTRONAIL TITANIUM UNIVERSAL FEMORAL NAILING SYSTEM
FDA UDI
ORTHOFIX SRL·18032568039634·RADIOLUCENT DRILL GUIDE D. 10/4.8 MM L. 165 MM
L070-0017 Tap Sleeve, Blackbird
FDA registration
Straits Orthopaedics (MFG) Sdn Bhd·1 product·🇲🇾 Malaysia
L070-0017 Tap Sleeve, Blackbird
FDA registration
STRAITS ORTHOPAEDICS (MFG) SDN BHD·1 product·🇲🇾 Malaysia
L070-0017 Tap Sleeve, Blackbird
FDA registration
STRAITS ORTHOPAEDICS (MFG) SDN BHD·1 product·🇲🇾 Malaysia
CULVER TOOL & ENGINEERING
FDA registration
CULVER TOOL & ENGINEERING·1 product·🇺🇸 United States
Synergy Health Ireland Ltd
FDA registration
Synergy Health Ireland Ltd·1 product·🇮🇪 Ireland
Blackbird Spinal System
FDA registration
Choice Spine·1 product·🇺🇸 United States
L070-0017 Tap Sleeve, Blackbird
FDA registration
STRAITS ORTHOPAEDICS (MFG) SDN BHD·1 product·🇲🇾 Malaysia
Acero Precision
FDA registration
Acero Precision·1 product·🇺🇸 United States
L070-0017 Tap Sleeve, Blackbird
FDA registration
STRAITS ORTHOPAEDICS (MFG) SDN BHD·1 product·🇲🇾 Malaysia
QuickVue TLI Campylobacter TEST
FDA registration
TECHLAB, INC.·1 product·🇺🇸 United States
Balloon - Extraction Fusion w multiple sizing injection port above - Biliary Catheter
FDA registration
PLATINUM FOCUS GROUP LTD.·1 product·🇬🇧 United Kingdom
Screw Driver Laminoplasty (L070-1001)
FDA registration
STRAITS ORTHOPAEDICS (MFG) SDN BHD·1 product·🇲🇾 Malaysia
M3810A PHILIPS TELEMONITORING SYSTEM WITH EDEVICE BRIDGED130
FDA 510(k)
FDA Class 2
·Cardiovascular
DUOWEDGE SYNTHETIC BONE SUBSTITUTE
FDA 510(k)
FDA Class 2
·Orthopedic