33 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Kyocera Bipolar Hip System
FDA 510(k)
FDA Class 2
·Orthopedic
Zavation
FDA UDI
Zavation LLC·00842166131811·Ti3Z CIF 12mmx14mmx9mm -7 deg
OsteoMed
FDA UDI
OSTEOMED LLC·00845694026093·1.6mm Pilot Drill, 22mm Stop
LFI POSTERIOR RETRACTOR, FLAT END 12MM & 16MM WIDTH
FDA UDI
W.H. Holden, Inc.·D9282007090·
ZAVATION
FDA UDI
Zavation LLC·00842166103900·CIF 12x14, 7 deg, -09
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756004428·POST-OP SHOE
BONASTENT® Tracheal/Bronchial
FDA UDI
Sewoon Medical Co., Ltd.·08806369469401·
Manta Ray TDF
FDA UDI
Seaspine Orthopedics Corporation·10889981287719·Manta Ray TDF Spacer, 16x14x9mm, 7 Deg, Strl Asm
Arena-C
FDA UDI
SPINEFRONTIER, INC.·00190361023029·12x15 Arena-C PEEK HA Straight 9mm
LFI POSTERIOR RETRACTOR, LONG FLAT END 12MM & 16MM WIDTH
FDA UDI
W.H. Holden, Inc.·D92820070910·
MODIFICATION TO CD HORIZON SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
EV1000 PLATFORM MODEL: EV1000A, EV1000DB, EV1000M
FDA 510(k)
FDA Class 2
·Cardiovascular
BD NANO¿ 2ND GEN PEN NEEDLES
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND CO.·Product code FMI·May 5, 2023
BD NANO¿ 2ND GEN PEN NEEDLES
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND CO.·Product code FMI·May 5, 2023
ALEUTIAN Interbody Systems
FDA UDI
VB Spine LLC·10888857188105·Disc Scraper Size 14 mm
BD NANO¿ 2ND GEN PEN NEEDLES 32G X 4MM (100 COUNT)
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND CO.·Product code FMI·June 9, 2023
BD NANO¿ 2ND GEN PEN NEEDLES 32G X 4MM (100 COUNT)
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND CO.·Product code FMI·June 9, 2023
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·December 30, 2015
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·May 1, 2014
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC, INC.·Product code KWP·August 1, 2011