PedFuse®

FDA UDI

SPINEFRONTIER, INC.·00190361011088·PedFuse RespondX, CNL, 6.0mm x 35mm

PedFuse®

FDA UDI

SPINEFRONTIER, INC.·00190361011095·PedFuse RespondX, CNL, 6.0mm x 40mm

PedFuse®

FDA UDI

SPINEFRONTIER, INC.·00190361011101·PedFuse RespondX, CNL, 6.0mm x 45mm

PedFuse®

FDA UDI

SPINEFRONTIER, INC.·00190361011125·PedFuse RespondX, CNL, 6.0mm x 55mm

TWIST DRILL

FDA UDI

Biomet Orthopedics, LLC·00887868017612·

ZELTIQ AESTHETICS CLN1 DERMAL COOLING DEVICE

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

STIMTRODE SINGLE USE NERVE STIMULATOR

FDA 510(k)

FDA Class 2 ·Anesthesiology

NA

FDA UDI

STERILMED, INC.·10888551009447·DRILL BIT

ClearGuard HD Antimicrobial barrier cap

FDA registration

ICU MEDICAL, INC·1 product·🇺🇸 United States

ISOMEDIX OPERATIONS INC.

FDA registration

ISOMEDIX OPERATIONS INC.·1 product·🇺🇸 United States

ClearGuard HD

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

CYDONIA PHARMA SL

FDA registration

CYDONIA PHARMA SL·1 product·🇪🇸 Spain

ClearGuard HD Antimicrobial barrier cap

FDA registration

ICU MEDICAL, INC.·1 product·🇺🇸 United States

Moellers Arginine Decarb

FDA registration

Hardy Diagnostics·1 product·🇺🇸 United States

ClearGuard HD Antimicrobial barrier cap

FDA registration

ICU MEDICAL, INC.·1 product·🇺🇸 United States

Fastener, Fixation, Nondegradable, Soft Tissue

FDA classification

FDA Class 2 ·Fastener, Fixation, Nondegradable, Soft Tissue

Stimulator, Nerve, Battery-Powered

FDA classification

FDA Class 2 ·Stimulator, Nerve, Battery-Powered

Powered Laser Surgical Instrument

FDA classification

FDA Class 2 ·Powered Laser Surgical Instrument