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

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CIRRUS HD-OCT

FDA 510(k)
FDA Class 2 ·Ophthalmic

X-CORE

FDA UDI
Nuvasive, Inc.·00887517300928·X-CORE 2 Ti Endcap, 22mm Rnd 0° Ø18

X-CORE

FDA UDI
Nuvasive, Inc.·00887517434685·X-CORE 2 Ti Endcap, 22mm Rnd 0° Ø22

FLEXIBLE REAMER SHAFT 2.0mm

FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665023688·

G185

FDA UDI
RESEARCH INSTRUMENTS LIMITED·05060554120109·Incubator for assisted reproduction

G185

FDA UDI
RESEARCH INSTRUMENTS LIMITED·05060554120116·Incubator for assisted reproduction

FLEXIBLE SHAFT

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·March 6, 2025

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523102099·R Tibial Baseplate Cemented Keeled Sz 2

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523101320·R Tibial Baseplate Cemented Stemmed Sz 2 Insert A

A3F FRATIONAL

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

PENTRA 120/PENTRA 120 RETIC OPTIONS SPS, MODEL PENTRA 120

FDA 510(k)
FDA Class 2 ·Hematology

FLEXIBLE SHAFT

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·August 25, 2025

Truliant

FDA UDI
Exactech, Inc.·10885862523747·TRULIANT POROUS TAMP HEAD

FLEXIBLE SHAFT

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·December 5, 2025

FLEXIBLE REAMER SHAFT, 2.0MM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·September 14, 2021

BIOMET SERIES A STANDARD PATELLA 28MM X 8.0MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JWH·August 24, 2011

OXIMAX N-560 PULSE OXIMETER

FDA Adverse Event
Malfunction ·MEDIANA·Product code DQA·November 3, 2014

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·July 12, 2013

NEEDLE FILTER BLUNT FILL 18X1-1/2

FDA Adverse Event
Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code GAA·February 28, 2020

TRUE METRIX

FDA Adverse Event
Malfunction ·TRIVIDIA HEALTH INC·Product code NBW·July 1, 2020