QBioscan

FDA registration

MEDEIA GROUP LTD·1 product·🇧🇬 Bulgaria

QBioscan

FDA registration

MEDEIA INC·1 product·🇺🇸 United States

QBioScan

FDA 510(k)

FDA Class 2 ·Neurology

Device, Galvanic Skin Response Measurement

FDA classification

FDA Class 2 ·Device, Galvanic Skin Response Measurement

MEDI

FDA UDI

MEDI MANUFACTURING, INC.·04051526768482·GENUMEDI PSS GREEN IV

MEDI

FDA UDI

MEDI MANUFACTURING, INC.·04064984699564·GENUMEDI PSS BLUE, SIZE IV

Biomet® Patellar System

FDA UDI

Biomet Orthopedics, LLC·00887868241659·

BIOMET PATELLAR SYSTEM

FDA UDI

Biomet Orthopedics, LLC·00880304240247·

AGXO

FDA UDI

Oticon A/S·05707131280671·H160V2, BTE 13 WL 85 SIL AGXO

AMT G-JET

FDA registration

STERILIZATION SERVICES OF GEORGIA, INC.·1 product·🇺🇸 United States

AESCULAP AG

FDA registration

AESCULAP AG·1 product·🇩🇪 Germany

Guidewire Accessory

FDA registration

Cosmed Group Inc.·1 product·🇺🇸 United States

Syringe accessory

FDA registration

APPLIED MEDICAL TECHNOLOGY, INC.·1 product·🇺🇸 United States

GUS ASTRA VR Endovaginal/Endorectal Probe Reprocesor

FDA registration

CIVCO Medical Instruments Co., Inc.·1 product·🇺🇸 United States

Synergy Health Ireland Ltd

FDA registration

Synergy Health Ireland Ltd·2 products·🇮🇪 Ireland

Boston Scientific Corporation

FDA registration

Boston Scientific Corporation·2 products·🇺🇸 United States

GUS ASTRA VR Endovaginal/Endorectal Probe Reprocesor

FDA registration

CIVCO Medical Instruments Co., Inc.·1 product·🇺🇸 United States

Synergy Health AST, SRL

FDA registration

Synergy Health AST, SRL·2 products·🇨🇷 Costa Rica

MODIFICATION TO: SPECTRUMTM CERVICAL SPINAL SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

AMT G-J TUBE

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology