10,000 results
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78ms
·
Sources: EU EUDAMED, US FDA
Action Trackchair HAWK
FDA registration
ATZ Manufacturing·1 product·🇺🇸 United States
Action Trackstander FALCON
FDA registration
ATZ Manufacturing·1 product·🇺🇸 United States
Action Trackchair EAGLE
FDA registration
ATZ Manufacturing·1 product·🇺🇸 United States
ATA HCM MONOPLACE HYPERBARIC SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
System, Hyperthermia, Rf/Microwave (Benign Prostatic Hyperplasia),Thermotherapy
FDA Pre-Market Approval
FDA Class 3
·TMX-2000 BPH THERMOTHERAPY SYSTEM
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·RADIESSE Injectable Implant, RADIESSE Hands, and RADIESSE (+) Lidocaine Dermal Filler
Agent, Bulking, Injectable For Gastro-Urology Use
FDA Pre-Market Approval
FDA Class 3
·COAPTITE Injectable Implant
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·RADIESSE Injectable Implant
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·ARCTIC FRONT CRYOABLATION CATHETER; ARCTIC FRONT ADVANCE CRYOABLATION CATHETER
Hepatitis A Test (Antibody And Igm Antibody)
FDA Pre-Market Approval
FDA Class 2
·HAVAB-M DIAGNOSTIC KIT
Hepatitis A Test (Antibody And Igm Antibody)
FDA Pre-Market Approval
FDA Class 2
·HAVAB-M EIA DIAGNOSTIC KIT
Barrier, Absorbable, Adhesion
FDA Pre-Market Approval
FDA Class 3
·INTERCEED ABSORBABLE ADHESION BARRIER
Agent, Absorbable Hemostatic, Non-Collagen Based
FDA Pre-Market Approval
FDA Class 3
·SURGICEL ABSORBABLE HEMOSTAT (SURGICEL, SURGICEL NU-KNIT AND SURGICEL FIBRILLAR ABSORBABLE HEMOSTATS)
MPS Power Cord Keeper
FDA UDI
QUEST MEDICAL INC·20634624510290·
Tissue Adhesive For Use In Embolization Of Brain Arteriovenous Malformations
FDA Pre-Market Approval
FDA Class 3
·TRUFILL n-BCA Liquid Embolic System
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·Clareon PanOptix Trifocal UV Absorbing Hydrophobic Intraocular Lens (IOL), Clareon PanOptix Toric Trifocal Hydrophobic I
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·MOBI-C CERVICAL DISC PROSTHESIS (TWO-LEVEL INDICATION)
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·MOBI-C CERVICAL DISC PROSTHESIS (ONE-LEVEL INDICATION)
System, Photopheresis, Extracorporeal
FDA Pre-Market Approval
FDA Class 3
·Therakos Cellex Photopheresis System
Reprieve by Regenesis
FDA UDI
Regenesis Biomedical, Inc.·00868924000038·The Reprieve by Regenesis device is a home-use ...