10,000 results
·
49ms
·
Sources: EU EUDAMED, US FDA
Barricaid
FDA registration
Intrinsic Therapeutics, Inc.·1 product·🇺🇸 United States
Sterigenics U.S., LLC
FDA registration
Sterigenics U.S., LLC·1 product·🇺🇸 United States
Sterigenics U.S., LLC
FDA registration
Sterigenics U.S., LLC·1 product·🇺🇸 United States
Barricaid® ACD (Annular Closure Device)
FDA UDI
INTRINSIC THERAPEUTICS, INC.·M906BARA88MM0·Barricaid® Annular Closure Device (ACD), 8mm wi...
Barricaid® ACD (Annular Closure Device)
FDA UDI
INTRINSIC THERAPEUTICS, INC.·M906BARA810MM0·Barricaid® Annular Closure Device (ACD), 10mm w...
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid® Annular Closure Device
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid Annular Closure Device
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid® Annular Closure Device
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid Anular Closure Device
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid Anular Closure Device (ACD)
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid® Annular Closure Device - Model Number BAR-A8-8MM (2730815-A&), Barricaid® Annular Closure Device - Model Numb
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·BARRICAID ANULAR CLOSURE DEVICE (ACD)
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid Annular Closure Device
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid Anular Closure Device
Reherniation Reduction Device
FDA classification
FDA Class 3
·Reherniation Reduction Device
EW-1, ES-1
FDA registration
CnS MEDICAL CO., LTD.·1 product·🇰🇷 South Korea
Ces Ultra
FDA registration
NEURO-FITNESS LLC·1 product·🇺🇸 United States
BES Srl
Manufacturer
🇮🇹 Italy
FLEX BT TRANSLUCENT
FDA registration
BES DEPOT, LLC·1 product·🇺🇸 United States
DLP SG Clear
FDA registration
BES DEPOT, LLC·1 product·🇺🇸 United States