34 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ZTT I AND II ACETABULAR CUP OF THE S-ROM TOTAL HIP SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Integra® Miltex®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780415152·Integra® Miltex® Universal Scissors, With Autoc...
BOWA
FDA UDI
Conmed Corporation·30845854081697·SHE SHA REF (950-000), Filter for 8 hours
Fresh Cells
FDA UDI
DIAGNOSTIC HYBRIDS, INC.·30014613331360·EMEM W/EBSS, HEPES, NO GLN
IPL HAIR REMOVAL DEVICE CT05
FDA Adverse Event
Injury
·SHENZHEN CHUANGTONG YIGOU TECHNOLOGY CO., LTD.·Product code OHT·February 19, 2026
HAND-HELD HAIR REMOVAL DEVICE
FDA Adverse Event
Injury
·SHENZHEN CHUANGTONG YIGOU TECHNOLOGY CO., LTD.·Product code OHT·March 9, 2026
7951000
FDA Adverse Event
Malfunction
·October 10, 2018
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756686228·SPONGE BOWL - BLUE
Sustainable Technologies
FDA UDI
Provision·00810041636089·Barrel bur; 6 flutes (tan; tan)
NA
FDA UDI
STERILMED, INC.·10888551030373·SHAVER BUR BARREL 6 FLUTE FORMULA SERIES TAN/TAN
NA
FDA UDI
Zimmer, Inc.·00889024183285·
Reprocessed 5.5mm Barrel Bur, 6 Flute
FDA UDI
SURETEK MEDICAL·B3903759510001·
NA
FDA UDI
Zimmer, Inc.·00889024183278·
Stryker
FDA UDI
Provision·B504AB3759510000·
N/A
FDA Adverse Event
Malfunction
·STRYKER SUSTAINABILITY SOLUTIONS, INC.·Product code HRX·June 9, 2017
FORTITUDE VUE VERTEBRAL BODY REPLACEMENT DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
O-Arm O2 Imaging System
FDA 510(k)
FDA Class 2
·Radiology
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756838245·SPONGE BOWL - RED
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756362894·SPONGE BOWL - BLUE
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756749282·SPONGE BOWL - RED