Prosthesis, Intervertebral Disc

FDA Pre-Market Approval

FDA Class 3 ·MOBI-C CERVICAL DISC PROSTHESIS (ONE-LEVEL INDICATION)

Prosthesis, Intervertebral Disc

FDA Pre-Market Approval

FDA Class 3 ·Mobi-C Cervical Disc Prosthesis for use at One or Two Levels

MILLER/GALANTE PRECOAT UNICOMPARTMENTAL KNEE

FDA registration

Sterigenics US, LLC·1 product·🇺🇸 United States

Zimmer Unicompartmental Knee Sys

FDA registration

Sterigenics US, LLC·1 product·🇺🇸 United States

NATURAL-KNEE TIBIAL AND FEMORAL SPACERS

FDA registration

Sterigenics US, LLC·1 product·🇺🇸 United States

MODIFICATION TO MILLER/GALANTE PRECOAT UNICOMPARTMENTAL KNEE SYSTEM (8 MM ARTICULAR SURFACE)

FDA registration

Sterigenics US, LLC·1 product·🇺🇸 United States

Persona Partial Knee System

FDA registration

Sterigenics US, LLC·1 product·🇺🇸 United States

INSALL/BURSTEIN(TM)* II TIBIAL WEDGES

FDA registration

Sterigenics US, LLC·1 product·🇺🇸 United States

MILLER/GALANTE PRECOAT UNICOMPARTMENTAL KNEE SYSTEM

FDA registration

Sterigenics US, LLC·1 product·🇺🇸 United States

BURNS CASUALTY SHEET LIMB WRAP

FDA 510(k)

FDA Class 1 ·General Hospital

BURNS CASUALTY SHEET BURN ROLL

FDA 510(k)

FDA Class 1 ·General Hospital

BURNS CASUALTY SHEET

FDA 510(k)

FDA Class 1 ·General Hospital

VIVACIT-E VITAMIN E HIGHLY CROSSLINKED ARTICULAR SURFACES

FDA registration

Sterigenics US, LLC·2 products·🇺🇸 United States

Bencox M Stem Lateralized & Bencox Mirabo Cup System

FDA 510(k)

FDA Class 2 ·Orthopedic

Bencox M Stem (Bencox Hip System) and Bencox ID Cemented Stem (with Centralizer) & Bencox Bone Plug

FDA 510(k)

FDA Class 2 ·Orthopedic

Bencox Mirabo Cup System

FDA 510(k)

FDA Class 2 ·Orthopedic

ZIMMER PATIENT SPECIFIC INSTRUMENTS PLANNER

FDA 510(k)

FDA Class 2 ·Orthopedic

Arthrex iBalance Partial Knee System

FDA 510(k)

FDA Class 2 ·Orthopedic

OMNIFIT TOTAL KNEE PROSTHESIS SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

MAKO SURGICAL UNICONDYLAR KNEE SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic