27 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.

BORRELIA BURGDORFERI IGG BLOT TEST

FDA 510(k)
FDA Class 2 ·Microbiology

SCREW SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304213982·

2870 3WAY SLIDE VALVE

FDA UDI
HANS RUDOLPH, INC.·00817136021959·2870/CLRA/2700 1.375 CP NO SMP

CapSure® Spine System

FDA UDI
Spine Wave, Inc.·10840642105360·PS3 Screw 8.5mm x 45mm

SMR SHOULDER SYSTEM - CTA HUMERAL HEADS

FDA 510(k)
FDA Class 2 ·Orthopedic

ANESTHESIA INJECTION TOOL SET

FDA 510(k)
FDA Class 2 ·Dental

UNIV RNGLC SHL 60MM/L23

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·November 3, 2020

UNKNOWN STEM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·November 3, 2020

RNGLC +5MM LNR 28MM HWALL SZ23

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·August 21, 2020

28MM DIA COCR MOD HD +9MM NK

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·August 21, 2020

NITE GUARD

FDA Adverse Event
Malfunction ·RANIR LLC·Product code OBR·May 1, 2014

PROLENE POLYPROPYLENE MESH

FDA Adverse Event
Injury ·ETHICON, INC.·Product code FTL·May 15, 2013

VASOVIEW HEMOPRO 2 EVH SYSTEM

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·May 17, 2011

BI-METRIC CDH POR N/C 7X114

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LZO·February 28, 2019

M2A 38MMX56MM CUP

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·February 28, 2019

M2A 38MM MOD HD -6MM NK

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·February 28, 2019

R3 XLPE INSERT

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code JDI·May 25, 2025

BI-METRIC CDH POR N/C 7X114

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·February 27, 2019

TITANIUM SCREW LOW PROF 5X25MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWS·February 27, 2019

TITANIUM SCREW LOW PROF 5X30MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWS·February 27, 2019