16 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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ACCULIF TL-PEEK IBF CAGE
FDA 510(k)
FDA Class 2
·Orthopedic
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613017699·K-Wire, Double Ended, Trocar Point, Diameter Si...
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756609975·Arm Sling
N/A
FDA UDI
MEDTRONIC XOMED, INC.·00763000913656·PROSTHESIS 1112095 H/A PARTL 90 OFF CTR
NA
FDA UDI
MEDTRONIC XOMED, INC.·00681490033398·PROSTHESIS 1112095 H/A PARTL 90 OFF CTR
N/A
FDA UDI
MEDTRONIC XOMED, INC.·00763000034733·PROSTHESIS 1112095 H/A PARTL 90 OFF CTR
n/a
FDA UDI
HANS RUDOLPH, INC.·00874750006090·2384A 2WAY TSHP NRBV .312/.250
Symmetry Wolfe-Boehler
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482054772·Symmetry® Breaker, Wolfe-Boehler Cast, 10 in
Integrity-SI Fusion System
FDA UDI
Lincotek Medical LLC·B57112521112095D0·12 x 95 mm Anodized SI Implant Fully Threaded
INFINION CX
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·May 13, 2024
SUSPENSION CLAVICLE FRACTURE FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
THE LPS - CONTINUUM TM HYBRID TIBIA, MODELS 32-5886-2Y-XX (ZIMMER) AND 05-119-XXYY1-0 (IMPLEX)
FDA 510(k)
FDA Class 2
·Orthopedic
INFINITI VISION SYSTEM OZIL
FDA Adverse Event
Malfunction
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·May 7, 2013
VISIAN ICL (IMPLANTABLE COLLAMER LENS)
FDA Adverse Event
Injury
·STAAR SURGICAL COMPANY·Product code HQL·June 2, 2011
CENTRA BED
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·August 6, 2008
INLIVEN CRT-P, Model Numbers: a) V284 b) V285 c) W274 d) W275 (added 7/15/2021)
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·July 21, 2021