UNICOMPARTMENTAL PATELLOFEMORAL PROSTHESIS (UPP) CEMENTED

FDA registration

BIOMET CHILE S.A.·1 product·🇨🇱 Chile

ZIMMER PTE. LTD.

FDA registration

ZIMMER PTE. LTD.·1 product·🇸🇬 Singapore

Zimmer (Shanghai) Medical International Trading Co., Ltd.

FDA registration

Zimmer (Shanghai) Medical International Trading Co., Ltd.·1 product·🇨🇳 China

Zimmer Biomet Pty Ltd

FDA registration

Zimmer Biomet Pty Ltd·1 product·🇦🇺 Australia

UNICOMPARTMENTAL PATELLOFEMORAL PROSTHESIS (UPP) CEMENTED

FDA registration

Zimmer Biomet Canada DFE·1 product·🇨🇦 Canada

Aragogamma, S.L.

FDA registration

Aragogamma, S.L.·1 product·🇪🇸 Spain

UNICOMPARTMENTAL PATELLOFEMORAL PROSTHESIS (UPP) CEMENTED

FDA registration

Biomet Global Supply Chain Center B.V.·1 product·🇳🇱 Netherlands

UNICOMPARTMENTAL PATELLOFEMORAL PROSTHESIS (UPP) CEMENTED

FDA 510(k)

FDA Class 2 ·Orthopedic

Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer

FDA classification

FDA Class 2 ·Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer

PowerPICC SOLO

FDA UDI

Bard Access Systems, Inc.·00801741152610·Catheter Placement Kit

AtriClip™ LAA Exclusion System

FDA UDI

ATRICURE, INC.·00818354011845·AtriClip® PRO Gillinov-Cosgrove LAA Exclusion S...

AtriClip™ LAA Exclusion System

FDA UDI

ATRICURE, INC.·10840143907210·AtriClip® PRO Gillinov-Cosgrove LAA Exclusion S...

AtriClip™ LAA Exclusion System

FDA UDI

ATRICURE, INC.·10840143901409·AtriClip® PRO Gillinov-Cosgrove LAA Exclusion S...

AtriClip® PRO Gillinov-Cosgrove LAA Exclusion System

FDA UDI

ATRICURE, INC.·10840143912054·LAA Exclusion System, PRO150

Cable

FDA UDI

Zoll Medical Corporation·00847946021856·VPAK, CABLE, PATIENT, X SERIES

UMBICUT

FDA registration

Euroband Bioline LTD.·2 products·🇮🇱 Israel

TriniCLOT Lupus Screen

FDA registration

TCOAG IRELAND LIMITED·1 product·🇮🇪 Ireland

TriniCLOT Lupus Screen

FDA registration

DIAGNOSTICA STAGO, INC.·1 product·🇺🇸 United States

acupuncture needles

FDA registration

HAENGLIM Co.,Ltd·1 product·🇰🇷 South Korea

INSUFFLATION NEEDLE, MODEL R65-933

FDA 510(k)

FDA Class 2 ·Obstetrics/Gynecology