29 results · 19ms · Sources: EU EUDAMED, US FDA

Monitor,Test,Hiv-1

FDA classification
FDA Class 3 ·Monitor,Test,Hiv-1

Implant, Dermal, For Aesthetic Use

FDA Pre-Market Approval
FDA Class 3 ·RESTYLANE/PERLANE/RESTYLANE-L/PERLANE-L INJECTABLE GELS

Tissue Graft Of 6mm And Greater

FDA Pre-Market Approval
FDA Class 3 ·ProCol Vascular Bioprosthesis

Excimer Laser System

FDA Pre-Market Approval
FDA Class 3 ·MEL 80 Excimer Laser

Excimer Laser System

FDA Pre-Market Approval
FDA Class 3 ·MEL 80 EXCIMER LASER SYSTEM

Excimer Laser System

FDA Pre-Market Approval
FDA Class 3 ·MEL 80 Excimer Laser System

Excimer Laser System

FDA Pre-Market Approval
FDA Class 3 ·MEL 80 Excimer Laser System

Excimer Laser System

FDA Pre-Market Approval
FDA Class 3 ·MEL 80 EXCIMER LASER SYSTEM

Excimer Laser System

FDA Pre-Market Approval
FDA Class 3 ·MEL 90 EXCIMER LASER SYSTEM

Excimer Laser System

FDA Pre-Market Approval
FDA Class 3 ·MEDITEC MEL 80 EXCIMER LASER SYSTEM

Lenses, Soft Contact, Extended Wear

FDA Pre-Market Approval
FDA Class 3 ·CSI (CROFILCON A) EXTENDED WEAR SOFT

Kit, Test, In Vitro Periodontal

FDA Pre-Market Approval
FDA Class 3 ·PERIOCHECK TM ENZYME ACTIVITY TEST KIT

Kit, Test, In Vitro Periodontal

FDA Pre-Market Approval
FDA Class 3 ·PERIOCHECK TM ENZYME ACTIVITY TEST KIT

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·MEDTRONIC(R) MDL 6966, 6936, 6963 TRANSVENE(R) AND MODEL 6939 AND 6999 SUBCUTANEOUS PATCH LEADS.

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·CADET V-105 C AND D AND V-115 C AND D PULSE GENERATORS & SOFTWARE VERSION 4.1 FOR THE PROGRAMMER MDL PR-1500

Prosthesis, Spinous Process Spacer/Plate

FDA Pre-Market Approval
FDA Class 3 ·COFLEX® INTERLAMINAR TECHNOLOGY

Prosthesis, Spinous Process Spacer/Plate

FDA Pre-Market Approval
FDA Class 3 ·COFLEX INTERLAMINAR TECHNOLOGY

Prosthesis, Spinous Process Spacer/Plate

FDA Pre-Market Approval
FDA Class 3 ·COFLEX INTERLAMINAR TECHNOLOGY

Prosthesis, Spinous Process Spacer/Plate

FDA Pre-Market Approval
FDA Class 3 ·COFLEX® INTERLAMINAR TECHNOLOGY

Prosthesis, Spinous Process Spacer/Plate

FDA Pre-Market Approval
FDA Class 3 ·coflex Interlaminar Stabilization Device