23 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Alinity h-series System
FDA 510(k)
FDA Class 2
·Hematology
CD HORIZON® Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994203649·CASE 7220031 SCREW GAUGE
LEONE SPA
FDA UDI
LEONE SPA·08033707022251·CALIBRA BANDS 2ND MOLAR n.SUR 31
Surface Electrode, Single-Pack
FDA UDI
Synapse Biomedical, Inc.·00852184003441·
Prosthesis, Spinous Process Tension Band Implant
FDA Pre-Market Approval
FDA Class 3
·LimiFlex Dynamic Sagittal Tether
DynaNail
FDA UDI
Medshape, Inc.·M97022003100000·DynaNail Carbon Fiber Frame 2.0 Assembly
EN-BLOC BIOPSY SYSTEM, MODELS 777-110, 777-120, 770-001, 777002, 777-006, 777-301, 777-302
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CHESAPEAKE SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
PANOSCREEN I, II, III
FDA Adverse Event
Malfunction
·IMMUCOR, INC.·Product code KSZ·June 15, 2011
Prosthesis, Spinous Process Tension Band Implant
FDA Pre-Market Approval
FDA Class 3
·LimiFlex Dynamic Sagittal Tether
BD VACUTAINER® SST¿
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code JKA·May 28, 2025
ITOTAL IDENTITY PS KNEE REPLACEMENT SYSTEM
FDA Adverse Event
Injury
·CONFORMIS INC.·Product code JWH·January 31, 2023
NA
FDA UDI
Zimmer, Inc.·00889024187115·
NA
FDA UDI
Zimmer, Inc.·00889024187078·
NA
FDA UDI
Zimmer, Inc.·00889024187085·
NA
FDA UDI
Zimmer, Inc.·00889024187092·
NA
FDA UDI
Zimmer, Inc.·00889024187122·
NA
FDA UDI
Zimmer, Inc.·00889024187108·
NA
FDA UDI
Zimmer, Inc.·00889024187139·
FLOGARD
FDA Adverse Event
Malfunction
·SHARP CORPORATION OSAKA JAPAN·Product code FRN·November 3, 2014