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

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APERIO EPATHOLOGY EIHC IVD SYSTEM

FDA 510(k)
FDA Class 2 ·Hematology

XLIF Decade Plate

FDA UDI
Nuvasive, Inc.·00887517316172·XLIF Decade Plate Counter Torque

Batrik Pin Guard\.109"\Beige

FDA UDI
Batrik Medical Manufacturing Inc·00690521011182·Pin Guard, .109" (2.77 mm), Beige, Non-sterile

Batrik Pin-Kaps

FDA UDI
Batrik Medical Manufacturing Inc·00690521014183·Pin-Kaps, Sterile, Beige, 0.109" / 2.77 mm

3M™ Unitek™

FDA UDI
3M UNITEK CORPORATION·00652221036803·Unitek(TM) Bicuspid Band General Purpose Narrow...

Batrik Pin Guard\.109"\Beige w/sleeve

FDA UDI
Batrik Medical Manufacturing Inc·00690521014589·Pin Guard, .109" (2.77 mm), Beige, Non-sterile,...

Plateau-C Spacer System

FDA UDI
Life Spine, Inc.·00190837011277·

Plateau-C Ti

FDA UDI
Life Spine, Inc.·00190837067113·Cement Restrictor, Straight, 9mm

EF1

FDA UDI
Medshape, Inc.·00810028398016·Pin Guard 7-64in 2.77mm Tan

VIVATRAK

FDA 510(k)
FDA Class 1 ·General Hospital

ZIMMER ANATOMIC II HIP PROSTHESIS

FDA 510(k)
FDA Class 2 ·Orthopedic

ClariVy™

FDA UDI
VY SPINE LLC·00840283400308·IBF Trial, 14x11, 9mm

CONTOUR

FDA Adverse Event
Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·October 14, 2011

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·June 13, 2024

SPECTRA WAVEWRITER?

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·May 30, 2025

BD ECLIPSE¿ HYPODERMIC NEEDLE

FDA Adverse Event
Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FMI·January 8, 2018

XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYSTEM

FDA Adverse Event
Malfunction ·AV-TEMECULA-CT·Product code NIQ·October 3, 2014

ASR UNI FEMORAL IMPL SIZE 46

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·June 3, 2013

OLYMPUS EVIS EXERA II BRONCHOVIDEOSCOPE

FDA Adverse Event
Other ·OLYMPUS MEDICAL SYSTEM CORPORATION·Product code EOQ·June 15, 2011

ENDOSKELETON® TO 4 DEG LORDOTIC, IMPLANT, 22X10MM, PLIF

FDA Adverse Event
Malfunction ·TITAN SPINE, LLC·Product code MAX·July 19, 2016