BeamPath GYN-L Fiber

FDA registration

Omni-Guide Holdings, Inc.·1 product·🇺🇸 United States

Omniguide2888 (NR) - URO-LG

FDA registration

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

OMNIGUIDE BEAM PATH CO2 MARK III WAVEGUIDE FIBER

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

ACS

FDA UDI

AMERICAN CONTRACT SYSTEMS, INC.·00191072037923·PACK CUSTOM C-SECTION SMHS - 2070157

Dalbo®-PLUS /-Classic /-B /-Z / Profix

FDA UDI

Cendres+Métaux SA·07640166514404·Dalbo®-PLUS /-Classic /-B /-Z / Profix Transfer...

CB Temp Temporary Crown & Bridge Material

FDA registration

J. MORITA USA, INC.·1 product·🇺🇸 United States

Synergy Sterilisation (M) Sdn Bhd

FDA registration

Synergy Sterilisation (M) Sdn Bhd·1 product·🇲🇾 Malaysia

WRP ASIA PACIFIC SDN. BHD.

FDA registration

WRP ASIA PACIFIC SDN. BHD.·1 product·🇲🇾 Malaysia

Zimmer

FDA UDI

Provision·B504TQ6070701570·

RegenerOss Allograft Putty

FDA registration

BIOMET 3i, LLC·1 product·🇺🇸 United States

RegenerOss Allograft Putty

FDA registration

Zimmer Biomet Dental Canada Inc.·1 product·🇨🇦 Canada

Synergy Health Ireland Ltd

FDA registration

Synergy Health Ireland Ltd·1 product·🇮🇪 Ireland

N/A

FDA UDI

STRYKER SUSTAINABILITY SOLUTIONS, INC.·00885825017675·Tourniquet Cuff with Sleeve Dual Port, Single B...

N/A

FDA UDI

ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024377219·ZIMMER® STERILE DISPOSABLE TOURNIQUET CUFF WITH...

POWDER FREE LATEX EXAMINATION GLOVES, STERILE WITH PROTEIN CONTENT LABELING CLAIM

FDA 510(k)

FDA Class 1 ·General Hospital

TEMPORARY CROWN AND BRIDGE MATERIAL

FDA 510(k)

FDA Class 2 ·Dental

Powered Laser Surgical Instrument

FDA classification

FDA Class 2 ·Powered Laser Surgical Instrument

Crown And Bridge, Temporary, Resin

FDA classification

FDA Class 2 ·Crown And Bridge, Temporary, Resin

Latex Patient Examination Glove

FDA classification

FDA Class 1 ·Latex Patient Examination Glove