22 results · 42ms · Sources: EU EUDAMED, US FDA

Sterigenics US LLC

FDA registration
Sterigenics US LLC·1 product·🇺🇸 United States

Endoskeleton TT IBD

FDA registration
PERRYMAN COMPANY·1 product·🇺🇸 United States

ENDOSKELETON TT INTERBODY FUSION DEVICE (IBD)

FDA registration
Medtronic Engineering and Innovation Center (MEIC)·1 product·🇮🇳 India

ENDOSKELETON TT INTERBODY FUSION DEVICE (IBD)

FDA registration
MEDTRONIC SOFAMOR DANEK USA, INC.·1 product·🇺🇸 United States

ENDOSKELETON TT INTERBODY FUSION DEVICE (IBD)

FDA registration
MEDTRONIC SOFAMOR DANEK USA, INC.·1 product·🇺🇸 United States

ENDOSKELETON TT INTERBODY FUSION DEVICE (IBD)

FDA registration
Medtronic Distribution Center·1 product·🇺🇸 United States

ENDOSKELETON TT INTERBODY FUSION DEVICE (IBD)

FDA registration
Titan Spine, a Division of Medtronic·1 product·🇺🇸 United States

ENDOSKELETON TT INTERBODY FUSION DEVICE (IBD)

FDA 510(k)
FDA Class 2 ·Orthopedic

appliance, fixation, nail/blade/plate combination, multiple component Reprocessed External Fixation Devices

FDA registration
Sterigenics US LLC·3 products·🇺🇸 United States

Isomedix Operations Inc.

FDA registration
Isomedix Operations Inc.·1 product·🇺🇸 United States

Reprocessed External Fixation Device

FDA registration
Stryker Sustainability Solutions·3 products·🇺🇸 United States

Reprocessed External Fixation Device

FDA registration
Stryker Sustainability Solutions Phoenix·3 products·🇺🇸 United States

Pronto LP Extraction Catheter. Model number 5010 - PRONTO LP 6F

FDA registration
Teleflex Medical de Tecate, S. de R.L de C.V.·1 product·🇲🇽 Mexico

Ag Positive Control ELISA

FDA registration
MONOCENT INC.·1 product·🇺🇸 United States

BinaxNOW Malaria Positive Control

FDA registration
Abbott Diagnostics Scarborough, Inc.·1 product·🇺🇸 United States

VASCULAR SOLUTIONS LLC

FDA registration
VASCULAR SOLUTIONS LLC·1 product·🇺🇸 United States

BinaxNOW Malaria Positive Control

FDA registration
ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·1 product·🇺🇸 United States

CODAN US I.V. ADMINISTRATION SET, MODEL B400 SP

FDA 510(k)
FDA Class 2 ·General Hospital

OSSTELL RESONANCE FREQUENCY ANALYZER

FDA 510(k)
FDA Class 1 ·Dental

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification
FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar