Vortex

FDA registration

LOUISIANA DENTAL IMPLANT LAB·1 product·🇺🇸 United States

MT-2

FDA 510(k)

FDA Class 2 ·Dental

P.F.C. SIGMA

FDA UDI

DEPUY ORTHOPAEDICS, INC.·10603295237679·P.F.C. SIGMA CURVED TIBIAL INSERT TRIAL SZ 6 17...

ONANON, INC

FDA registration

ONANON, INC·1 product·🇺🇸 United States

Shockwave7578 (PT, SDB) - Lithoplasty Peripheral Balloon Dilatation Catheter

FDA registration

Synergy Health AST, LLC·1 product·🇺🇸 United States

Shockwave Medical, Inc. Peripheral Lithoplasty System

FDA registration

SHOCKWAVE MEDICAL, INC.·1 product·🇺🇸 United States

LORENZ PECTUS SUPPORT BAR STABILIZER, TITANIUM

FDA registration

Changzhou Biomet Medical Devices Co., Ltd.·1 product·🇨🇳 China

Shockwave Medical Lithoplasty (R) System

FDA registration

VANGUARD-EMS·1 product·🇺🇸 United States

Shockwave7578 (PT, SDB) - Lithoplasty Peripheral Balloon Dilatation Catheter

FDA registration

Synergy Health AST, LLC·1 product·🇺🇸 United States

LORENZ PECTUS SUPPORT BAR STABILIZER, TITANIUM

FDA registration

BIOMET, INC.·1 product·🇺🇸 United States

Shockwave7578 (PT, SDB) - Lithoplasty Peripheral Balloon Dilatation Catheter

FDA registration

Synergy Health AST, SRL·1 product·🇨🇷 Costa Rica

Pectus Bar System

FDA registration

BIOMET MICROFIXATION·1 product·🇺🇸 United States

LORENZ PECTUS SUPPORT BAR, TITANIUM; LORENZ PECTUS SUPPORT BAR STABILIZER, TITANIUM

FDA 510(k)

FDA Class 2 ·Orthopedic

Lithoplasty Peripheral Balloon Dilatation Catheter, Lithoplasty Generator and Connector Cable, Lithoplasty Connector Cable

FDA 510(k)

FDA Class 2 ·Cardiovascular

Percutaneous Catheter, Ultrasound

FDA classification

FDA Class 2 ·Percutaneous Catheter, Ultrasound

Implant, Endosseous, Root-Form

FDA classification

FDA Class 2 ·Implant, Endosseous, Root-Form

Plate, Fixation, Bone

FDA classification

FDA Class 2 ·Plate, Fixation, Bone