28 results · 21ms · Sources: EU EUDAMED, 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