25 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Avanti
FDA 510(k)
FDA Class 2
·Ophthalmic
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197537094·Titanium Ryder Needle Holder
diamon...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197085311·Titanium Ryder Needle Holder
diamon...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197085304·Titanium Ryder Needle Holder
diamon...
INFRARED EAR THERMOMETER MODEL DR. SCHVEN ICT-1000
FDA 510(k)
FDA Class 2
·General Hospital
IV ADMINISTRATION SET
FDA 510(k)
FDA Class 2
·General Hospital
LOCKING SCREW, FULLY THREADED 5X55 MM
FDA Adverse Event
Injury
·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·September 30, 2010
BIOLOX DELTA CER LNR 36MM E
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LZO·February 5, 2026
RINGLOC-X E1 H/W 56/36MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·April 27, 2026
BIOLOX DELTA CER LNR 40MM G
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·April 27, 2026
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 15, 2014
VIBRANT SOUNDBRIDGE
FDA Adverse Event
Malfunction
·VIBRANT MED-EL HEARING TECHNOLOGY GMBH·Product code MPV·May 5, 2011
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·June 20, 2013
AVAN E1 INSERT 28 S 52
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·March 6, 2025
BIOLOX DELTA CER LNR 32MM E
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·September 8, 2025
RINGLOC BIPOLAR VIVACIT-E
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code LPH·September 10, 2025
6.5/8.0mm Cannulated Screw System, BCS Cannulated Screw System (3.0, 4.0/5.0, 6.5/8.0mm), Item numbers 110009929, 110009934, 110009935, 110009936, 110009993, 110009994, 110009996, 110009998, 110010000, 110010003, 110010029, 110010030, 110010032, 110010099 - Product Usage: Fracture fixationof small bones, small bone fragements and long bones.
FDA Enforcement
Class II
·Terminated·Biomet, Inc.·December 23, 2020
MW5072527
FDA Adverse Event
Injury
·September 29, 2017
BIOLOX DELTA CER LNR 36MM E
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·November 13, 2025
BIOLOX DELTA LNR 40MM 58-60MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·August 21, 2025