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

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BIORAPTOR CURVED 2.3 PK SUTURE ANCHORS

FDA 510(k)
FDA Class 2 ·Orthopedic

TALOS® IBF

FDA UDI
MEDITECH SPINE, LLC·B16741026600·

TALOS® IBF

FDA UDI
MEDITECH SPINE, LLC·B1674102660060·

Dornier MedTech

FDA UDI
Dornier MedTech GmbH·04049957000011·R- Compact Sigma Lithotripter, 120V, 60 Hz

Zavation

FDA UDI
Zavation LLC·00842166150072·10x26x60mm, 0°, MILC

Zavation

FDA UDI
Zavation LLC·00842166150829·10x26x60mm, 6°, MILC

HARDYDISK LOMEFLOXACIN, 10MCG

FDA 510(k)
FDA Class 2 ·Microbiology

GIMMI'ALPHA' ENDOSCOPES & ACCESSORIES

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

SMR HUMERAL HEAD Ø48 MM

FDA Adverse Event
Injury ·LIMACORPORATE S.P.A.·Product code KWT·January 27, 2023

AXOGUARD NERVE CONNECTOR AND PROTECTOR

FDA Adverse Event
Injury ·COOK BIOTECH·Product code JXI·August 24, 2015

SYNCHROMED II

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·May 9, 2013

PLUM A+ DRIVER ED 2

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·August 28, 2014

TERUMO PERFUSION SYSTEM 8000

FDA Adverse Event
Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP·Product code DTQ·May 23, 2011

CMK OC - RASP S303

FDA Adverse Event
Malfunction ·BIOMET UK LTD.·Product code LZO·January 28, 2026

CMK OC - RASP S303

FDA Adverse Event
Malfunction ·BIOMET UK LTD.·Product code LZO·January 28, 2026

CMK OC - RASP S202

FDA Adverse Event
Malfunction ·BIOMET UK LTD.·Product code LZO·February 5, 2026

CMK OC - RASP S302

FDA Adverse Event
Malfunction ·BIOMET UK LTD.·Product code LZO·February 5, 2026

CMK OC - RASP S303

FDA Adverse Event
Malfunction ·BIOMET UK LTD.·Product code LZO·January 28, 2026

CMK OC - RASP S302

FDA Adverse Event
Malfunction ·BIOMET UK LTD.·Product code LZO·February 5, 2026

CMK OC - RASP S401

FDA Adverse Event
Malfunction ·BIOMET UK LTD.·Product code LZO·February 5, 2026