OMNIPORE DUROMAX ZB Orbital Implant

FDA registration

MATRIX SURGICAL HOLDINGS, LLC dba MATRIX SURGICAL USA·1 product·🇺🇸 United States

OmniPore DUROMAX Surgical Implants

FDA 510(k)

FDA Class 2 ·Dental

Long Pulse Nd: YAG Laser System

FDA registration

BEIJING WINKONLASER TECHNOLOGY LIMITED·1 product·🇨🇳 China

Trojan Charged Condom

FDA registration

CHURCH & DWIGHT CO., INC.·1 product·🇺🇸 United States

Trojan Charged Condom

FDA registration

Church & Dwight Manufacturing Co., Inc.·1 product·🇺🇸 United States

Diazyme 1,5 Anhydroglucitol (1,5 AG) Control Set

FDA registration

Diazyme Laboratories, Inc.·1 product·🇺🇸 United States

Xiros8315 (DV) - Infinity-Lock Button System

FDA registration

SYNERGY HEALTH STERILISATION UK LTD·1 product·🇬🇧 United Kingdom

Plate, Bone

FDA classification

FDA Class 2 ·Plate, Bone

FLOR-OPAL VARNISH WHITE; MODELS 4503, 4504, 4506, S4505

FDA 510(k)

FDA Class 2 ·Dental

TROJAN MAGNUM CONDOM WITH WARMING LUBRICANT

FDA 510(k)

FDA Class 2 ·Obstetrics/Gynecology

CANNULATED CANCELLOUS LAG SCREW, REDUCED HEAD

FDA UDI

Biomet Orthopedics, LLC·00887868017933·

CANNULATED CANCELLOUS LAG SCREW, REDUCED HEAD

FDA UDI

Biomet Orthopedics, LLC·00887868018008·

CANNULATED CANCELLOUS LAG SCREW, REDUCED HEAD

FDA UDI

Biomet Orthopedics, LLC·00887868018107·

CANNULATED CANCELLOUS LAG SCREW, REDUCED HEAD

FDA UDI

Biomet Orthopedics, LLC·00887868017964·

CANNULATED CANCELLOUS LAG SCREW, REDUCED HEAD

FDA UDI

Biomet Orthopedics, LLC·00887868017957·

CANNULATED CANCELLOUS LAG SCREW, REDUCED HEAD

FDA UDI

Biomet Orthopedics, LLC·00887868018022·

CANNULATED CANCELLOUS LAG SCREW, REDUCED HEAD

FDA UDI

Biomet Orthopedics, LLC·00887868018015·

CANNULATED CANCELLOUS LAG SCREW, REDUCED HEAD

FDA UDI

Biomet Orthopedics, LLC·00887868018138·

CANNULATED CANCELLOUS LAG SCREW, REDUCED HEAD

FDA UDI

Biomet Orthopedics, LLC·00887868017926·

CANNULATED CANCELLOUS LAG SCREW, REDUCED HEAD

FDA UDI

Biomet Orthopedics, LLC·00887868018114·