9 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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STELKAST ALL POLYETHYLENE ACETABULAR CUP
FDA 510(k)
FDA Class 2
·Orthopedic
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471122376·K-WIRE - SINGLE TROCAR THREADED 1.6mm DIA x 230mm
3M™ Victory Series™
FDA UDI
3M UNITEK CORPORATION·00652221116352·3M™ Victory Series™ First Molar Bands, 953-169,...
PASS OCT Patient Specific Rods
FDA 510(k)
FDA Class 2
·Orthopedic
RM3 RENAL PRESERVATION SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PULSE-GENERATOR, PACEMAKER, IMPLANTABLE
FDA Adverse Event
Injury
·RICE CREEK MFG·Product code DXY·February 9, 2013
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·January 7, 2011
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·July 23, 2014
CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026