26 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Impress Angiographic Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
Audina
FDA UDI
Bernafon AG·05711584086421·CAPTO 5 B 105, 2.4G NFM DPB JEBL AUDIN
OneLIF™
FDA UDI
Novapproach Spine LLC·G07001021916080·OneLIF Interbody, Medium, 19 Degree, 16mm X 8mm
OneLIF™
FDA UDI
Novapproach Spine LLC·G07001121916080·Trial-OneLIF Interbody, Medium, 19 Degree, 16mm...
Vacutron
FDA UDI
Allied Medical, LLC·00026072010747·Mini-Vac
COBALT MV BONE CEMENT
FDA 510(k)
FDA Class 2
·Orthopedic
BIOMET 3I PATIENT SPECIFIC DENTAL ABUTMENTS-ENCODE ABUTMENTS
FDA 510(k)
FDA Class 2
·Dental
ILAB POLARIS MULTI-MODALITY GUIDANCE SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DQK·March 3, 2025
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076331287·Trial, 19x16mm, 8mm height, 6-degree
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076336596·Trial, 19x16mm, 8mm height, 12-degree stopless
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076330969·Trial, 19x16mm, 8mm height,
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076336039·Trial, 19x16mm, 8mm height, 12-degree
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076331614·Rasp, 19x16mm, 8mm height, 6-degree
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076330273·3D Porous Titanium Cervical Interbody, 19x16mm,...
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076336879·Rasp, 19x16mm, 8mm height, 12-degree stopless
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076335759·3D Porous Titanium Cervical Interbody, 19x16mm,...
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076336312·Rasp, 19x16mm, 8mm height, 12-degree
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076330594·3D Porous Titanium Cervical Interbody, 19x16mm,...
ILAB? POLARIS MULTI-MODALITY GUIDANCE SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DQK·May 14, 2026
AZUR VASCULAR PLUG 8
FDA Adverse Event
Injury
·MICROVENTION, INC.·Product code KRD·March 29, 2022