22 results
·
22ms
·
Sources: EU EUDAMED, US FDA
TOPSLANE DMLC
FDA 510(k)
FDA Class 2
·Radiology
Mini-Mono®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR70601871·Mini-Mono-Brackets Roth 'N' .018" 200 Brackets ...
SAFE-T-FILL®
FDA UDI
Ram Scientific, Inc·10643351000281·SAFE-T-FILL Plastic Blood Gas Capillary Tubes, ...
REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
KIMAX, MODEL 1024
FDA 510(k)
FDA Class 2
·Radiology
PHILOS II DR
FDA Adverse Event
Injury
·BIOTRONIK GMBH AND CO.·Product code DXY·September 1, 2006
SELOX SR 45
FDA Adverse Event
Injury
·BIOTRONIK GMBH AND CO.·Product code DTB·September 1, 2006
LIFESTENT FLEXSTAR XL BILIARY STENT
FDA Adverse Event
Injury
·ANGIOMED GMBH & CO.·Product code FGE·November 21, 2008
LIFESTENT FLEXSTAR XL BILIARY STENT
FDA Adverse Event
Malfunction
·ANGIOMED GMBH & CO.·Product code FGE·November 5, 2008
LIFESTENT FLEXSTAR XL BILIARY STENT
FDA Adverse Event
Malfunction
·ANGIOMED GMBH & CO. MEDIZINTECHNIK·Product code FGE·February 20, 2009
LIFESTENT FLEXSTAR XL BILIARY STENT
FDA Adverse Event
Malfunction
·ANGIOMED GMBH & CO.·Product code FGE·November 4, 2008
LIFESTENT FLEXSTAR XL BILIARY STENT
FDA Adverse Event
Malfunction
·ANGIOMED GMBH & CO, MEDIZINTECHNIK·Product code FGE·February 13, 2009
JUVEDERM ULTRA PLUS XC TSK ROW
FDA Adverse Event
Injury
·ALLERGAN·Product code LMH·April 11, 2013
OSCILLATING SAW BLADE
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS·Product code DWH·May 19, 2008
GYNECARE MORCELLEX* TISSUE MORCELLATOR
FDA Adverse Event
Malfunction
·ETHICON·Product code HET·April 15, 2011
SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 230 ¿L; Prepared with Balanced Heparin, Model/Catalog Number: 06 0187 Product Description: A clear, plastic capillary blood collection tube
FDA Enforcement
Class II
·Ongoing·ASP Global, LLC. dba Anatomy Supply Partners, LLC.·November 26, 2025
EVOLUT FX VALVE
FDA Adverse Event
Injury
·MEDTRONIC MEXICO S. DE R.L. DE CV·Product code NPT·July 9, 2025
SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 230 L; Prepared with Balanced Heparin, Model/Catalog Number: 06 0187 Product Description: A clear, plastic capillary blood collection tube
FDA Recall
Open, Classified
·ASP Global, LLC. dba Anatomy Supply Partners, LLC.·Product code GIO·September 26, 2025
KLS Martin Cranial Implants - MR Conditional; K944565: KLS-Martin Micro Osteosynthesis System (1.5MM); K971297: KLS Martin Centre-Drive Drill-Free Screw; K060177: KLS Martin Rigid Fixation - Sterile; K062570: Individual Patient Solutions - Ti (IPS-Ti); K072707: Individual Patient Solutions - PEEK (IPS-PEEK) ; K151382: Individual Patient Solutions - (IPS-PEEK) - STERILE
FDA 510(k)
FDA Class 2
·Neurology
Instructions For Use document of the GPS Trackers.
FDA Enforcement
Class II
·Terminated·Blue Ortho·November 4, 2020