25 results · 23ms · Sources: EU EUDAMED, 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