11 results
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25ms
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Sources: EU EUDAMED, US FDA
NON CONDUCTIVE, SINGLE USE ANESTHESIA FACE MASK
FDA 510(k)
FDA Class 1
·Anesthesiology
Signature
FDA UDI
SILEX MEDICAL, LLC·B3315881067·Locking Maryland Dissecting Forceps
Snowden-Pencer
FDA UDI
STERIS CORPORATION·10885403151545·Snowden-Pencer FREEMAN RAKE RETRACTOR X-SMALL, ...
Signature
FDA UDI
SILEX MEDICAL, LLC·B331588106745·Locking Long Maryland Dissecting Forceps
LinkSymphoKnee - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575310258·Medullary canal orthopaedic reamer, rigid - Lin...
AlignX Ankle Fusion System
FDA 510(k)
FDA Class 2
·Orthopedic
FRACTURE/RECONSTRUCTION SYSTEM (TRAUMAONE)
FDA 510(k)
FDA Class 2
·Dental
BURR, OVAL,SJ, 10 FLUTE, 3.0MM X 7CM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code GFF·June 18, 2014
PROLIFT PELVIC FLOOR REPAIR
FDA Adverse Event
Injury
·ETHICON, INC.·Product code FTL·October 19, 2010
R SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·November 9, 2012
BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026