XULTAN 5.5 REDUCTION PEDICLE SCREW 5.5 X 35 MM CANN

FDA UDI

MET 1 TECHNOLOGIES, LLC·00819824022187·THE XULTAN 5.5 PEDICLE SCREW SYSTEM IS AN IMPLA...

08x26x0° KODIAK PLIF TRIAL

FDA UDI

MET 1 TECHNOLOGIES, LLC·00819824028813·The Met One Technologies Kodiak Lumbar Spacer S...

CZAR VARIABLE SELF TAPPING SCREW 4.5

FDA UDI

MET 1 TECHNOLOGIES, LLC·00819824024785·THE MET ONE CZAR ANTERIOR CERVICAL PLATE SYSTEM...

08x27x0° KODIAK TLIF TRIAL

FDA UDI

MET 1 TECHNOLOGIES, LLC·00819824029117·The Met One Technologies Kodiak Lumbar Spacer S...

KODIAK CORPECTOMY IMPLANT, 14x16mm, 27mmx6°

FDA UDI

MET 1 TECHNOLOGIES, LLC·00819824027113·THE MET ONE TECHNOLOGIES KODIAK C SPINAL VERTEB...

AUDERE C CORPECTOMY IMPLANT 56MM X 6°

FDA UDI

MET 1 TECHNOLOGIES, LLC·00819824020459·THE AUDERE C SPINAL INTERVETEBRAL BODY FUSION D...

XULTAN 5.5 PEDICLE SCREW 8.5 X 35 MM CANN

FDA UDI

MET 1 TECHNOLOGIES, LLC·00819824021869·THE XULTAN 5.5 PEDICLE SCREW SYSTEM IS AN IMPLA...

XULTAN 5.5 PEDICLE ROD 30 MM BENT

FDA UDI

MET 1 TECHNOLOGIES, LLC·00819824023238·THE XULTAN 5.5 PEDICLE SCREW SYSTEM IS AN IMPLA...

CZAR ANTERIOR CERVICAL PLATE SYSTEM 4 LEVEL

FDA UDI

MET 1 TECHNOLOGIES, LLC·00819824024402·THE MET ONE CZAR ANTERIOR CERVICAL PLATE SYSTEM...

12x14mm, 5mmx0° KODIAK CERVICAL TRIAL

FDA UDI

MET 1 TECHNOLOGIES, LLC·00819824027496·THE MET ONE TECHNOLOGIES KODIAK C SPINAL INTERV...

XULTAN 5.5 PEDICLE ROD 80 MM BENT

FDA UDI

MET 1 TECHNOLOGIES, LLC·00819824023337·THE XULTAN 5.5 PEDICLE SCREW SYSTEM IS AN IMPLA...

AUDERE C CORPECTOMY IMPLANT 48 MM X 6°

FDA UDI

MET 1 TECHNOLOGIES, LLC·00819824020374·THE AUDERE C SPINAL INTERVETEBRAL BODY FUSION D...

AUDERE POSTERIOR LUMBAR SPACER SYSTEM

FDA UDI

MET 1 TECHNOLOGIES, LLC·00819824020787·THE AUDERE POSTERIOR LUMBAR SPACER SYSTEM CONSI...

Automated External Defibrillators (Non-Wearable)

FDA Pre-Market Approval

FDA Class 3 ·HeartSine Technologies LLC's samaritan Public Access Automated External Defibrillators and Accessories

Automated External Defibrillators (Non-Wearable)

FDA Pre-Market Approval

FDA Class 3 ·HeartSine Technologies LLC's samaritan Public Access Automated External Defibrillators and Accessories

108.7800 - MASTERtorque LUX M8900 L

FDA registration

KAVO DENTAL GMBH·1 product·🇩🇪 Germany

MRPen MicroSystem

FDA registration

GUANGZHOU CARAIN BEAUTY EQUIPMENT·1 product·🇨🇳 China

100.4672 - PROPHYflex 3 2018 black

FDA registration

KAVO DENTAL GMBH·1 product·🇩🇪 Germany

107016 - PROPHYflex powder cherry

FDA registration

KAVO DENTAL GMBH·1 product·🇩🇪 Germany

109.8757 - Tube Set S600

FDA registration

KAVO DENTAL GMBH·1 product·🇩🇪 Germany