26 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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RenovoCath
FDA 510(k)
FDA Class 2
·Cardiovascular
Audina
FDA UDI
Bernafon AG·05711584086407·CAPTO 5 B 105, 2.4G NFM DPB MSIL AUDIN
OneLIF™
FDA UDI
Novapproach Spine LLC·G07001131916060·Trial-OneLIF Interbody, Large, 19 Degree, 16mm ...
OneLIF™
FDA UDI
Novapproach Spine LLC·G07001031916060·OneLIF Interbody, Large, 19 Degree, 16mm X 6mm
Vacutron
FDA UDI
Allied Medical, LLC·00026072010730·Mini-Vac
VERTAPLEX HV (SINGLE PACK AND DUAL PACK)
FDA 510(k)
FDA Class 2
·Orthopedic
MICROMED PD-8K INSULATION DEFECT DETECTOR
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 19, 2020
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076331591·Rasp, 19x16mm, 6mm height, 6-degree
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076336015·Trial, 19x16mm, 6mm height, 12-degree
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076330945·Trial, 19x16mm, 6mm height,
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076330259·3D Porous Titanium Cervical Interbody, 19x16mm,...
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076336855·Rasp, 19x16mm, 6mm height, 12-degree stopless
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076331263·Trial, 19x16mm, 6mm height, 6-degree
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076336299·Rasp, 19x16mm, 6mm height, 12-degree
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076335735·3D Porous Titanium Cervical Interbody, 19x16mm,...
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076330570·3D Porous Titanium Cervical Interbody, 19x16mm,...
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076336572·Trial, 19x16mm, 6mm height, 12-degree stopless
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·October 22, 2014
DEPUY ASR XL FEM IMP SIZE 49
FDA Adverse Event
Injury
·DEPUY INTL., LTD. - 8010379·Product code KXA·June 26, 2013