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

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COLLAGEN-ORC ANTIMICROBIAL MATRIX

FDA 510(k)
FDA Unclassified ·Unknown

5.4 Dual-Port Mixing Tips (50-pack)

FDA UDI
CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172000703·Dental material mixing nozzle, non-sterile

5.4 Dual-Port Mixing Tips 50-Pack

FDA UDI
DEN-MAT HOLDINGS, LLC·00359883002633·Dental material mixing nozzle, non-sterile

Baltic Denture System BDLoad

FDA UDI
Merz Dental GmbH·D7091033523·Baltic Denture System BDLoad BDLoad ↓ Ln6 PLSEu...

DEPUY PINNACLE METAL-ON-METAL ACETABULAR CUP LINERS

FDA 510(k)
FDA Class 3 ·Orthopedic

CISTEM FLUID TRANSFER DEVICE, MODEL 7S2012 AND 7S2013

FDA 510(k)
FDA Class 2 ·General Hospital

D 903 AVANT ADULT HOLLOW FIBER OXYGENATOR

FDA Adverse Event
Other ·SORIN GROUP ITALIA·Product code DTZ·February 27, 2014

D903 DIDECO AVANT 2 VAVD PHISIO

FDA Adverse Event
Other ·SORIN GROUP ITALIA·Product code DTZ·February 19, 2014

IT PADOVA

FDA Adverse Event
Other ·SORIN GROUP ITALIA·Product code DTZ·August 8, 2013

D903 DIDECO AVANT VAVD PHISIO

FDA Adverse Event
Other ·SORIN GROUP ITALIA·Product code DTZ·August 16, 2013

HOMECHOICE AUTOMATED PD SET WITH CASSETTE

FDA Adverse Event
Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·April 3, 2013

OCTRODE PERCUTANEOUS TRIAL LEAD

FDA Adverse Event
Injury ·ST JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·March 24, 2011

ACCU-CHEK SPIRIT

FDA Adverse Event
Malfunction ·DISETRONIC MEDICAL SYSTEMS·Product code LZG·April 23, 2008

C20441 IL HAIFA

FDA Adverse Event
Other ·SORIN GROUP ITALIA·Product code DWF·March 28, 2012

PROGREAT

FDA Adverse Event
Malfunction ·TERUMO MEDICAL CORPORATION·Product code DQO·March 5, 2024

TERUMO PROGREAT CATHETER

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQO·February 6, 2023

PROGREAT CATHETER

FDA Adverse Event
Malfunction ·TERUMO MEDICAL CORPORATION·Product code DQO·January 6, 2024

PROGREAT

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQO·April 15, 2025

ENDURANT II STENT GRAFT

FDA Adverse Event
Malfunction ·MEDTRONIC IRELAND·Product code MIH·November 1, 2023

ENDURANT II STENT GRAFT

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code MIH·November 1, 2023