30 results
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38ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MOTO PFJ System
FDA 510(k)
FDA Class 2
·Orthopedic
MOTO PARTIAL KNEE ANATOMICAL FEMORAL COMPONENT CEMENTED S5 RM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code HSX·March 8, 2024
Integra® Jarit®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780165279·Integra® Jarit® Parker Retractor, 7", Double-En...
The Inseminator
FDA UDI
Coopersurgical, Inc.·00888937011494·Intrauterine Inseminator, 3.5 French, 4.5" Long...
Ophthalmic Cannula
FDA UDI
KATENA PRODUCTS, INC.·00841668113899·VISCO INJECTION CANNULA 26GA
Sonoma™
FDA UDI
Seaspine Orthopedics Corporation·10889981050764·Sonoma Anterior Cervical Plate 1 Level Plate, 22mm
Initia Total Hip System
FDA UDI
KYOCERA MEDICAL CORPORATION·04580810057914·"MXHO LINER 28-60/64
Size:28-60/62/64
Type:Elev...
Initia Total Hip System
FDA UDI
KYOCERA CORPORATION·04547898307744·MXHO LINER 28-60/64
PHOENIX SFS
FDA UDI
Orthofix US LLC·18257200009145·GUIDE WIRE, NITINOL, 19.5", SHARP
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306804939·Sheehan Osteotome, 2mm, 16cm
Manta Ray™
FDA UDI
Seaspine Orthopedics Corporation·10889981057015·Plate - 1 Level - 22 mm
NA
FDA UDI
aap Implantate AG·04042409079948·Cortical Screw 2.0, L 22
COLLAGRAFT STRIP BONE GRAFT MATRIX (FOR USE AS A BONE FILLER), MODEL 1X,3X,6X (1,3 OR 6 STRIPS PER BOX)
FDA 510(k)
FDA Class 2
·Orthopedic
MB 102 MILLENNIUM BLADES
FDA 510(k)
FDA Class 1
·Ophthalmic
COMPRESSURE FRACTURE REPAIR IMPLANT
FDA Adverse Event
Injury
·USI ORTHOPAEDICS LLC DBA U.S. ORTHOPAEDICS·Product code HTN·April 6, 2011
NA
FDA UDI
aap Implantate AG·04042409079955·Cortical Screw 2.0, L 22
HNM MEDICAL
FDA UDI
HNM STAINLESS, LLC.·00842962160190·PICCOLO AUTOCLAVABLE PLASTIC TRAY, 9"X6"X2", LO...
ARCHITECT I1000SR
FDA Adverse Event
Malfunction
·ABBOTT LABORATORIES·Product code JJE·December 19, 2022
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·August 10, 2011
ACCU-CHEK COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·October 15, 2008