11 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ProKnow DS
FDA 510(k)
FDA Class 2
·Radiology
Bernafon
FDA UDI
Bernafon AG·05711584081495·ZERENA 9 MNR T FW 1.0
UNIVERSAL IRRIGATION SOLUTION HYBRID
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MENICON PROGENT PROTEIN REMOVER FOR RIGID GAS PERMEABLE CONTACT LENSES
FDA 510(k)
FDA Class 2
·Ophthalmic
6000CMS
FDA Adverse Event
Malfunction
·MOOG DEVICE GROUP·Product code FRN·June 11, 2013
SEQUOIA FINAL DRIVER (PLE)
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 8, 2011
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·October 17, 2014
WILSON-COOK ACHALASIA BALLOON
FDA Adverse Event
Injury
·COOK ENDOSCOPY·Product code PID·June 17, 2021
PREVENA PLUS INCISION MANAGEMENT SYSTEM
FDA Adverse Event
Injury
·KINETIC CONCEPTS, INC·Product code OMP·September 24, 2021
Talar Dome Total Ankle Prosthesis , Sloped, Size 1, Right, Product No. LJV181T
FDA Enforcement
Class II
·Terminated·Integra LifeSciences Corp.·April 24, 2019
WILSON-COOK ACHALASIA BALLOON
FDA Adverse Event
Malfunction
·COOK ENDOSCOPY·Product code PID·October 6, 2020