18 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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STARband, STARlight, St. Louis Band
FDA 510(k)
FDA Class 2
·Neurology
STERICAN™
FDA UDI
B. BRAUN MEDICAL INC.·04046964354427·21 Ga. x 7/8 in. Blunt Cannula Needle
Super Upper Limbs Versalock Plating System
FDA UDI
GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258665665·VERSALOCK TOTAL WRIST FUSION PLATE - SHORT ANG...
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361010654·PedFuse Reset, SLD, 6.0mm x 35mm
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361010647·PedFuse Reset, SLD, 6.0mm x 30mm
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361010678·PedFuse Reset, SLD, 6.0mm x 45mm
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361010685·PedFuse Reset, SLD, 6.0mm x 50mm
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361010692·PedFuse Reset, SLD, 6.0mm x 55mm
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361010661·PedFuse Reset, SLD, 6.0mm x 40mm
MW5084161
FDA Adverse Event
February 19, 2019
VANISHPOINT INSULIN SYRINGE
FDA Adverse Event
Malfunction
·RETRACTABLE TECHNOLOGIES, INC.·Product code MEG·October 2, 2018
LOGIFLEX LAPAROSCOPIC BAND POSITIONING DEVICE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
SYNTHES (USA) MODULAR BLADE PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Coaxial needle
FDA UDI
Möller Medical GmbH·04260277178123·
CHARGING SYS
FDA Adverse Event
Injury
·ST JUDE MED - NEUROMODULATION·Product code GZB·October 15, 2014
MCA LARGE APPLIER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDO·July 27, 2011
OUTLOOK ES
FDA Adverse Event
Malfunction
·B. BRAUN MEDICAL, INC.·Product code FRN·June 13, 2013
INSET 30
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·November 18, 2025