14 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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RADIOSCOPE OR MAMMOSCOPE
FDA 510(k)
FDA Class 2
·Radiology
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690197881·AK3 PS-C Insert Trial Size 4, 12mm
Empower 2®
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746011474·DB BKT SL EMPOWER PASSIVE LR 1ST BICUSPID 018 ...
Empower 2®
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746008498·DB BKT SL EMPOWER INTERACT LR 1ST BICUSPID 018...
Empower Bracket
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746132537·DB BKT SL EMPOWER PASSIVE LR 1ST BIC 018 T-12 A...
Empower Bracket
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746141171·DB BKT SL EMPOWER INTERACT LR 1ST BIC 018 T-12 ...
THE PROTECTOR
FDA 510(k)
FDA Class 1
·Anesthesiology
PRESERV PVA FIXATIVE 15ML-FORMALIN PK
FDA 510(k)
FDA Class 1
·Pathology
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FKX·June 25, 2014
ABBOTT AXSYM SYSTEM
FDA Adverse Event
Malfunction
·ABBOTT MANUFACTURING, INC.·Product code JJE·November 9, 2010
REVERTO
FDA Adverse Event
Malfunction
·CORE ESSENCE ORTHOPAEDICS·Product code JDR·December 27, 2012
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·June 21, 2024
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·June 21, 2024
GMK-REVISION FEMUR REVISION PS SIZE 2 R
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·February 7, 2020