SCREW

FDA registration

DePuy Mitek, Inc.·1 product·🇺🇸 United States

TITANIUM CANNULATED INTERFERENCE SCREW

FDA 510(k)

FDA Class 2 ·Orthopedic

NVM5

FDA UDI

Nuvasive, Inc.·00887517141095·NVM5 PM, 2+SSEPs

LEONE SPA

FDA UDI

LEONE SPA·08033707066231·PREFORMED LIGATURE WIRE 012"

2040 Ceramic Brackets

FDA UDI

AMERICAN ORTHODONTICS CORPORATION·00190746005367·COSMETIC 20/40 MAND ANTERIOR 022 T=0 A=0 R=0

AESCULAP AG

FDA registration

AESCULAP AG·1 product·🇩🇪 Germany

AESCULAP, INC.

FDA registration

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

PEPIN MFG., INC.

FDA registration

PEPIN MFG., INC.·1 product·🇺🇸 United States

christoph miethke gmbh & co.kg

FDA registration

christoph miethke gmbh & co.kg·1 product·🇩🇪 Germany

Monitor, breathing frequency

FDA registration

DYMEDIX DIAGNOSTICS INC·1 product·🇺🇸 United States

CHRISTOPH MIETHKE GMBH & CO.KG

FDA registration

CHRISTOPH MIETHKE GMBH & CO.KG·1 product·🇩🇪 Germany

ULTRAPOWER

FDA UDI

Conmed Corporation·10845854002520·6.5MM ULTRAPOWER BUR, ROUND (RED)

SMARTLOOP

FDA registration

Fx Shoulder Solutions SAS·1 product·🇫🇷 France

Reusable Neonatal Hand/Foot SpO2 Sensor (1.5m)

FDA registration

Volcano Corporation by Volcarica S.R.L.·1 product·🇨🇷 Costa Rica

RESPIRATORY BELT SENSOR, MODEL 6000S; LIMB MOVEMENT SENSOR, MODEL 3000S

FDA 510(k)

FDA Class 2 ·Anesthesiology

AESCULAP -MIETHKE SHUNT SYSTEM

FDA 510(k)

FDA Class 2 ·Neurology

Screw, Fixation, Bone

FDA classification

FDA Class 2 ·Screw, Fixation, Bone

Monitor, Breathing Frequency

FDA classification

FDA Class 2 ·Monitor, Breathing Frequency

Shunt, Central Nervous System And Components

FDA classification

FDA Class 2 ·Shunt, Central Nervous System And Components