28 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Tria Soft Ureteral Stent
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Audina
FDA UDI
Bernafon AG·05711584086438·CAPTO 5 B 105, 2.4G NFM DPB MAC/MSIL AUDIN
ARSENAL PETITE LAPIDUS PLATE, R
FDA Adverse Event
Injury
·TRILLIANT SURGICAL·Product code HRS·April 3, 2020
OneLIF™
FDA UDI
Novapproach Spine LLC·G07001111916090·Trial-OneLIF Interbody, Small, 19 Degree, 16mm ...
General Instruments
FDA UDI
ALPHATEC SPINE, INC.·00840180543719·TLIF Slides w/ 1/4" Sq Backend, 9mm Wide
OneLIF™
FDA UDI
Novapproach Spine LLC·G07001011916090·OneLIF Interbody, Small, 19 Degree, 16mm X 9mm
SELF RETAINING SOFT TISSUE RETRACTOR
FDA 510(k)
FDA Class 1
·Orthopedic
NEWDEAL COMPRESSION PLATE
FDA 510(k)
FDA Class 2
·Orthopedic
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076336886·Rasp, 19x16mm, 9mm height, 12-degree stopless
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076331294·Trial, 19x16mm, 9mm height, 6-degree
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076330280·3D Porous Titanium Cervical Interbody, 19x16mm,...
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076330600·3D Porous Titanium Cervical Interbody, 19x16mm,...
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076330976·Trial, 19x16mm, 9mm height,
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076335766·3D Porous Titanium Cervical Interbody, 19x16mm,...
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076336602·Trial, 19x16mm, 9mm height, 12-degree stopless
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076336329·Rasp, 19x16mm, 9mm height, 12-degree
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076331621·Rasp, 19x16mm, 9mm height, 6-degree
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076336046·Trial, 19x16mm, 9mm height, 12-degree
2800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 20, 2011
ASR UNI FEMORAL IMPL SIZE 43
FDA Adverse Event
Injury
·DEPUY INTL., LTD. - 8010379·Product code KWA·June 26, 2013