29 results
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38ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TempTraq
FDA 510(k)
FDA Class 2
·General Hospital
Blade Handle
FDA UDI
KATENA PRODUCTS, INC.·00841668112397·BARD-PARKER HANDLE #9
HYBRID FS & HYBRID FS TORIC (HYCOFOCON A) RGP CONTACT LENS FOR DAILY WEAR
FDA 510(k)
FDA Class 2
·Ophthalmic
TAPERED SCREW-VENT T IMPLANT
FDA 510(k)
FDA Class 2
·Dental
IMP,TSV,4.7,10,MTX,MG
FDA Adverse Event
Injury
·ZIMVIE US CORP LLC·Product code DZE·May 22, 2026
IMP,TSV,4.7,11.5,MTX,MG
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·June 12, 2024
IMP,TSV,4.7,10,MTX,MG
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·October 28, 2024
IMP,TSV,4.7,8,MTX,MG
FDA Adverse Event
Injury
·ZIMVIE US CORP LLC·Product code DZE·April 22, 2026
IMP,TSV,6.0,11.5,MTX,MG
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·May 15, 2025
IMP,TSV,3.7,8,MTX,MG
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·July 12, 2024
IMP,TSV,4.7,10,MTX,MG
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·June 10, 2024
OCTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·October 17, 2014
VASO VIEW HEMOPRO
FDA Adverse Event
Injury
·MAQUET CARDIOVASCULAR, LLC·Product code GEI·August 5, 2011
SPEEDSTITCH SUTURING DEVICE
FDA Adverse Event
Malfunction
·ARTHROCARE CORPORATION·Product code GAT·June 27, 2013
IMP,TSV,4.7,11.5,MTX,MG
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·November 6, 2024
IMP,TSV,4.7,8,MTX,MG
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·November 8, 2024
IMPL TAPERED SCR-V SBM 3. 7MM 3.5MM 8MM
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·October 4, 2023
MICRA
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code PNJ·February 21, 2020
IMP,TSV,4.7,8,MTX,MG
FDA Adverse Event
Injury
·ZIMVIE US CORP LLC·Product code DZE·March 17, 2026
PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code NEW·May 10, 2022