6019

FDA registration

R & D BATTERIES, INC.·1 product·🇺🇸 United States

BATTER PACK, REPLACEMENT FOR PHYSIO CONTROL LIFEPAK 500

FDA 510(k)

FDA Class 3 ·Cardiovascular

Biomet Knee System

FDA UDI

Biomet Orthopedics, LLC·00880304233065·

Applied Medical Distribution Center

FDA registration

Applied Medical Distribution Center·1 product·🇺🇸 United States

APPLIED MEDICAL RESOURCES CORP.

FDA registration

APPLIED MEDICAL RESOURCES CORP.·1 product·🇺🇸 United States

Applied Medical Europe

FDA registration

Applied Medical Europe·1 product·🇳🇱 Netherlands

Renu

FDA registration

ADVASAF LLC·1 product·🇺🇸 United States

Cytophil, Inc

FDA registration

Cytophil, Inc·1 product·🇺🇸 United States

Automated External Defibrillators (Non-Wearable)

FDA classification

FDA Class 3 ·Automated External Defibrillators (Non-Wearable)

Delta TT Jumbo Cups

FDA registration

Limacorporate S.p.A.·4 products·🇮🇹 Italy

Coag Endo-Dissector

FDA registration

Ovesco Endoscopy USA·1 product·🇺🇸 United States

Coag Endo-Dissector

FDA registration

OVESCO ENDOSCOPY AG·1 product·🇩🇪 Germany

MODIFICATION TO OPTICAL SEPARATOR SYSTEM

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

CALCIUM HYDROXYLAPATITE VOCAL FOLD IMPLANT

FDA 510(k)

FDA Class 2 ·Ear, Nose, Throat

System, Vocal Cord Medialization

FDA classification

FDA Class 2 ·System, Vocal Cord Medialization

Laparoscope, General & Plastic Surgery

FDA classification

FDA Class 2 ·Laparoscope, General & Plastic Surgery