22 results · 22ms · Sources: EU EUDAMED, US FDA

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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