15 results · 32ms · Sources: EU EUDAMED, US FDA

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SIMPLASTIC SUPRA PUBIC CATHETER

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

APEX Knee System

FDA UDI
Omni Life Science, Inc.·00841690192169·Apex Revision Knee Reamer – ZIMMER SHORT FLUTES...

Rapid Molar Intruder

FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746133268·RMI RAPID MOLAR INTRUDER KIT OF 5 PAIRS

SurgTech Interbody System

FDA 510(k)
FDA Class 2 ·Orthopedic

TEM 3000 HEAD COIL

FDA 510(k)
FDA Class 2 ·Radiology

PINNACLE SECTOR II CUP 54MM

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·October 31, 2013

MERIDIAN TMZF HIP STEM #3/13MM

FDA Adverse Event
Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LZO·June 5, 2014

ENDOTAK RELIANCE

FDA Adverse Event
Injury ·CPI - DEL CARIBE·Product code NVY·October 4, 2010

HEARTSINE SAMARITAN SAM 300P AND PAD PAK

FDA Adverse Event
Death ·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·November 26, 2012

TI LOW PROFILE SCREW 6.5X20MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·October 15, 2025

M/H RADIAL 3-HOLE SHELL 52MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LZO·October 15, 2025

TI LOW PROFILE SCREW 6.5X40MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·October 15, 2025

PINNACLE MTL INS NEUT36IDX54OD

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·September 19, 2013

ARTICULEZE M HEAD 36MM +5

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·September 19, 2013

Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.

FDA Enforcement
Class II ·Terminated·STERILMED, INC.·December 16, 2015