13 results
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34ms
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Sources: EU EUDAMED, US FDA
STORZ E9050 & E9055 DIAMOND KNIVES
FDA 510(k)
FDA Class 1
·Ophthalmic
Vyaire
FDA UDI
Jaeger Medical GmbH·14250892906451·Flow Restrictor
Vyaire
FDA UDI
Jaeger Medical GmbH·14250892903757·Flow Restrictor
Jaeger
FDA UDI
Jaeger Medical GmbH·14250892902200·Flow Restrictor
Jaeger
FDA UDI
Jaeger Medical GmbH·14250892907571·Flow Restrictor
JOBST Maternity
FDA UDI
BSN MEDICAL, INC.·04042809641912·OPAQUE MATERNITY 15-20 MM HG THIGH HIGH ZIG ZAG...
TAP-T
FDA 510(k)
FDA Class 2
·Dental
PRISMA-FIL
FDA 510(k)
FDA Class 2
·Dental
PD CYCLER 110 VOLT HOME CHOICEPRO AUTOMATED
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·October 8, 2010
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 13, 2014
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·December 7, 2012
MINIMED QUICK-SET
FDA Adverse Event
Malfunction
·UNOMEDICAL UM-D·Product code FPA·January 13, 2025
OEC 6800 Miniview, Image-intensified fluoroscopic x-ray system used during diagnostic, surgical and interventional procedures. Designed to provide the physician with general fluoroscopic visualization of the patient including but not limited to surgical orthopedic and extremity imagine. The device is not intended for whole-body pediatric imaging.
FDA Enforcement
Class I
·Terminated·GE OEC Medical Systems, Inc·August 1, 2012