30 results · 24ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

SYNTHES MATRIXMADIBLE PLATE AND SCREW SYSTEM

FDA 510(k)
FDA Class 2 ·Dental

SYRINGE 1.0ML 29GA 1/2IN 200BX1600 HP CA

FDA Adverse Event
Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·June 8, 2020

TM2000 FETALTRACE TRANSTELEPHONIC RECEIVING CENTER

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

ARK GABAPENTIN ASSAY, ARK GABEPENTIN CALIFRATOR, AND ARK GABAPENTIN CONTROL MODEL5025-0001-00, 5025-0002-00, 5025-0003-0

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

G7 SCREW

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code PBI·June 2, 2017

AVAN CMNTD SHELL SS 50MM

FDA Adverse Event
Malfunction ·BIOMET UK LTD.·Product code LZO·April 24, 2026

MODULAR CUP SYSTEM, RIMCUP

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018

RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018

AVAN CMNTD SHELL SS 50MM

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code LZO·January 21, 2026

RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018

RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018

VICTORY XL DR

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWP·January 13, 2014

ACCU-CHEK SPIRIT

FDA Adverse Event
Malfunction ·ROCHE DIABETES CARE AG·Product code LZG·May 21, 2013

PFC SIGMA/OV/DOME PAT 3PEG, 38

FDA Adverse Event
Injury ·DEPUY (IRELAND)·Product code JWH·June 2, 2011

RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018

G7 BONEMASTER LTD ACET SHL 58G

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code JDI·September 23, 2019

G7 FINNED BM 3 HOLE SHELL 48C

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code JDI·May 16, 2018

DURAL ALPHA INSERT NEUTR JJ/36

FDA Adverse Event
Malfunction ·ZIMMER GMBH·Product code LZO·February 18, 2026

G7 BONEMASTER LTD ACET SHL 46B

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code PBI·July 18, 2019

G7 BONEMASTER LTD ACET SHL 52E

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·May 14, 2018