10,000 results
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96ms
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Sources: EU EUDAMED, US FDA
Spectacle, magnifying
FDA registration
WENZHOU INRAY OPTICAL CO., LTD·1 product·🇨🇳 China
Frame, spectacle
FDA registration
WENZHOU INRAY OPTICAL CO., LTD·1 product·🇨🇳 China
Lens, spectacle, non-custom (prescription)
FDA registration
WENZHOU INRAY OPTICAL CO., LTD·1 product·🇨🇳 China
Sunglasses (non-prescription including photosensitive)
FDA registration
WENZHOU INRAY OPTICAL CO., LTD·1 product·🇨🇳 China
Accu-O-Matic
FDA UDI
ETD Electro-Therapeutic Devices Inc·00628235150057·Advance Transcutaneous Electrical Nerve Stimulator
SafeCross Transseptal RF Puncture and Steerable Balloon Introducer System
FDA UDI
East End Medical I LLC·08600035053013·SafeCross Transseptal RF Puncture and Steerable...
SafeCross Transseptal RF Puncture and Steerable Balloon Introducer System
FDA UDI
East End Medical I LLC·08600035053037·SafeCross Transseptal RF Puncture and Steerable...
SafeCross Transseptal RF Puncture and Steerable Balloon Introducer System
FDA UDI
East End Medical I LLC·08600035053020·SafeCross Transseptal RF Puncture and Steerable...
Saliva, Artificial
FDA Pre-Market Approval
FDA Unclassified
·SALIVART
Signum liquid
FDA registration
KULZER GMBH·2 products·🇩🇪 Germany
Ortho-Choice Ortho-Coat
FDA registration
PULPDENT CORPORATION·2 products·🇺🇸 United States
AGEE-WRISTJACK FRACTURE REACTION SYSTEM (STERILE VERSION), MODEL CFD-147
FDA 510(k)
FDA Class 2
·Orthopedic
KYPHON® Bone Filler Device (BFD)
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169335868·BONE FILLER DEVICE F04B SIZE 3-RB
KYPHON® Bone Filler Device (BFD)
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00763000311650·BONE FILLER DEVICE F04B SIZE 3-RB
Salice
FDA registration
SALICE OCCHIALI SRL·1 product·🇮🇹 Italy
Salice
FDA registration
SALICE OCCHIALI SRL·1 product·🇮🇹 Italy
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·AID (R) B/BR HIGH VOLTAGE CABLES FOR ECD SYSTEMS
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·EFH-16; S60-K; S 60-J; S 60-S
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·EFH-16; S 60-K; S 60-J; S 60-S
ClearGuard HD
FDA UDI
Pursuit Vascular, Inc.·B081CGHD106236579·ClearGuard HD end caps are blood access device ...