2,256 results · 25ms · Sources: EU EUDAMED, US FDA

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Endoskeleton TA Interbody Fusion Device, Endoskeleton TAS and TAS Hyperlordotic Interbody Fusion Device, Endoskeleton TO Interbody Fusion Device, Endoskeleton TT Interbody Fusion Device, Endoskeleton TC Interbody Fusion Device, Endoskeleton TCS Interbody Fusion Device, Endoskeleton TL Interbody Fusion Device

FDA 510(k)
FDA Class 2 ·Orthopedic

Echo® Bi-Metric® Hip System

FDA UDI
Biomet Orthopedics, LLC·00887868260490·

ECHO BI-METRIC HIP SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304462939·

Bernafon

FDA UDI
Bernafon AG·05711584086926·ZR3, KIT 312 NFM R BE ZERENA 3

OsteoMed

FDA UDI
OSTEOMED LLC·00845694009621·2.0mm x 18mm Cannulated Lag Screw

Instrument Case

FDA UDI
KATENA PRODUCTS, INC.·00841668110935·STERILIZING CASE NARROW

OsteoMed

FDA UDI
OSTEOMED LLC·00845694070249·Cannulated 2.0 x 18mm Lag Screw Sterile Qty 5

OMNIPRO INCLINE

FDA 510(k)
FDA Class 2 ·Radiology

NORIAN REINFORCED, NORIAN REINFORCED FAST SET PUTTY

FDA 510(k)
FDA Class 2 ·Neurology

MENTOR MEMORYGEL BREAST IMPLANT

FDA Adverse Event
Injury ·MENTOR TEXAS·Product code FTR·April 11, 2018

640G INSULIN PUMP MMT-1711K

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·September 29, 2022

ARTICUL/EZE BALL 28 + 1.5 GR

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL, LTD.·Product code JDI·October 6, 2008

ZIMMER M/L TAPER FEMORAL STEM

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code LZO·June 20, 2013

SCULPTRA

FDA Adverse Event
AVENTIS PHARMA GRUPPO LEPETIT S.R.L.·Product code LMH·July 29, 2011

HEARTWARE VENTRICULAR ASSIST SYSTEM - CONTROLLER 2.0

FDA Adverse Event
Malfunction ·HEARTWARE, INC.·Product code DSQ·February 22, 2018

ANIMAS VIBE

FDA Adverse Event
Malfunction ·ANIMAS LLC·Product code OYC·July 5, 2018

ANIMAS VIBE

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code OYC·January 11, 2018

DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code PQF·March 21, 2018

BA400 ABUTMENT 10MM

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·June 18, 2018

BIA400 IMPLANT 4MM

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·January 18, 2018