22 results
·
44ms
·
Sources: EU EUDAMED, US FDA
INSTRU-MED TECHNOLOGIES
FDA registration
INSTRU-MED TECHNOLOGIES·1 product·🇺🇸 United States
SPINAL ELEMENTS, INC.
FDA registration
SPINAL ELEMENTS, INC.·1 product·🇺🇸 United States
Lucent®
FDA 510(k)
FDA Class 2
·Orthopedic
ACS
FDA UDI
AMERICAN CONTRACT SYSTEMS, INC.·00191072160515·DW INTERVENTIONAL RADIO PACK - 170235
ACS
FDA UDI
AMERICAN CONTRACT SYSTEMS, INC.·00191072017338·DW INTERVENTIONAL RADIO PACK - 170235
ACS
FDA UDI
AMERICAN CONTRACT SYSTEMS, INC.·00191072100368·DW INTERVENTIONAL RADIO PACK - 170235
ACS
FDA UDI
AMERICAN CONTRACT SYSTEMS, INC.·00191072155818·DW INTERVENTIONAL RADIO PACK - 170235
3M ESPE DENTAL PRODUCTS
FDA registration
3M ESPE DENTAL PRODUCTS·1 product·🇺🇸 United States
JERSEY DENTAL SUPPLIES
FDA registration
JERSEY DENTAL SUPPLIES·1 product·🇺🇸 United States
MAINLINE MEDICAL DENTAL SUPPLY
FDA registration
MAINLINE MEDICAL DENTAL SUPPLY·1 product·🇨🇦 Canada
Neo Elite
FDA registration
MEDICAL LASER TECHNOLOGIES LTD.·1 product·🇷🇺 Russian Federation
SANICURE BV
FDA registration
SANICURE BV·1 product·🇳🇱 Netherlands
EEKAY LOGISTICS LLC
FDA registration
EEKAY LOGISTICS LLC·1 product·🇺🇸 United States
3M ESPE Dental Products
FDA registration
3M ESPE Dental Products·1 product·🇺🇸 United States
NORTH AMERICAN WHOLESALERS LLC
FDA registration
NORTH AMERICAN WHOLESALERS LLC·1 product·🇺🇸 United States
Neo Elite
FDA registration
AEROLASE CORPORATION·1 product·🇺🇸 United States
BONE GRAFTING MATERIAL, HUMAN
FDA registration
SWEDEN & MARTINA INC·1 product·🇺🇸 United States
BODYGUARD PAIN MANAGER INFUSION SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
FILTEK SUPREME ULTRA FLOWABLE RESTORATIVE
FDA 510(k)
FDA Class 2
·Dental
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar