Premofix

Device

EU MDR · Eu Md Class 1 ·Andanza International, Inh. Ulrich Östreicher e.K.·On the market

Premofix

Device

EU MDR · Eu Md Class 1 ·Andanza International, Inh. Ulrich Östreicher e.K.·On the market

Premofix

Device

EU MDR · Eu Md Class 1 ·Andanza International, Inh. Ulrich Östreicher e.K.·On the market

Premofix

Device

EU MDR · Eu Md Class 1 ·Andanza International, Inh. Ulrich Östreicher e.K.·On the market

LEJA

FDA registration

LEJA PRODUCTS B.V.·1 product·🇳🇱 Netherlands

APEX Spine System

FDA UDI

SPINECRAFT, LLC·00193082051203·T20 Self-Retaining Driver, No Handle

Scan abutment Engaging GM H 15.0

Device

EU MDR · Eu Md Class 1 ·IMPLANT PROTESIS DENTAL 2004 S.L.·On the market·22 countries

Scan abutment Engaging GM H 10.0

Device

EU MDR · Eu Md Class 1 ·IMPLANT PROTESIS DENTAL 2004 S.L.·On the market·22 countries

UNO 30

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

UNO Negative Pressure Wound Therapy System

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

UNO Negative Pressure Wound Therapy System

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

SERI Contour

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

PATIENT EXAMINATION GLOVES

FDA 510(k)

FDA Class 1 ·General Hospital

PATIENT EXAMINATION GLOVES (LATEX)

FDA 510(k)

FDA Class 1 ·General Hospital

NATURAL RUBBER LATEX MALE CONDOMS

FDA 510(k)

FDA Class 2 ·Obstetrics/Gynecology

MALE LATEX CONDOM (STRAIGHT SIDE OR CONTOURED OR FLARED IN SHAPE, EITHER TEXTURED OR NON-TEXTURED , LUBRICATED OR NON-LU

FDA 510(k)

FDA Class 2 ·Obstetrics/Gynecology

Quantum Mitohormesis (QMT) (M2101)

FDA 510(k)

FDA Class 2 ·Physical Medicine

LATEX EXAMINATION GLOVES

FDA 510(k)

FDA Class 1 ·General Hospital

RUBBER CONTRACEPTIVE

FDA 510(k)

FDA Class 2 ·Obstetrics/Gynecology

Silk Voice

FDA 510(k)

FDA Class 2 ·Ear, Nose, Throat