89 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MODEL B-200 C-ARM & MODEL C-300 CARDIAC TABLE
FDA 510(k)
FDA Class 2
·Radiology
HOTWIRE™ RF GUIDEWIRE
FDA UDI
Atraverse Medical, Inc·00850057445305·The HOTWIRE™ is a sterile, single-use guidewire...
NA
FDA UDI
Stryker GmbH·04546540414502·Metal Screw Rack
OsteoVation
FDA UDI
SKELETAL KINETICS LLC·00813845020054·OsteoVation Inject Bone Void Filler
PeritX
FDA UDI
Bard Peripheral Vascular, Inc.·00801741230615·PeritX™ 2L Drainage Starter Tote
Symmetry Surgical
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482151914·Symmetry® Scissors; 5 mm x 350 mm; Blunt; Taper...
Triton
FDA UDI
ASI MEDICAL, INC.·00850309007077·Triton Dental System
Elite®
FDA UDI
Ortho Organizers, Inc.·00190707051143·.018 U6R STD/NC -14T 5 OFF
ALLURA XPER OR TABLE SERIES
FDA 510(k)
FDA Class 2
·Radiology
BOLUSPRO ULTRA
FDA 510(k)
FDA Class 2
·Radiology
VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·November 19, 2019
OIC INTRAMEDULLARY NAIL SYSTEM
FDA Adverse Event
Malfunction
·ORTHOPAEDIC IMPLANT COMPANY, THE·Product code HSB·October 21, 2020
PROLENE POLYPROPYLENE MESH UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code FTL·March 16, 2019
PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAW·March 16, 2019
VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·March 16, 2019
PROLENE HERNIA SYSTEM UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code FTL·March 16, 2019
OSTEOVATION INJECT 5CC
FDA Adverse Event
Other
·SKELETAL KINETICS, LLC·Product code GXP·November 25, 2009
TTP J-TUBE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC·Product code FPD·April 6, 2007
OSTEOVATION IMPACT 5CC AND INJECT 5CC
FDA Adverse Event
Malfunction
·SKELETAL KINETICS, LLC·Product code GXP·November 25, 2009
SYMBIQ SCHANNEL 3.01
FDA Adverse Event
Malfunction
·HOSPIRA HOLDINGS DE COSTA RICA LTD.·Product code FRN·May 7, 2014