156 results · 28ms · Sources: EU EUDAMED, US FDA

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COBALT V RADIOPAQUE VERTEBROPLASTY BONE CEMENT

FDA 510(k)
FDA Class 2 ·Orthopedic

Paltop

FDA UDI
PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290108690354·Titanium Straight Abutment Internal Hex. SP Ø5....

EVOS Lumbar Interbody System

FDA UDI
Cutting Edge Spine, LLC·00841193105048·HA PEEK EVOS Curved, , 15mmx10mmx 26mm , BICONV...

Paltop

FDA UDI
PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290108690149·Advanced Dental Implant Ø5mm L13mm

Aligned Medical Solutions

FDA UDI
Aligned Medical Solutions·B09800700150·PERI PACK

SYNOX 53-15 BP

FDA Adverse Event
Injury ·BIOTRONIK GMBH AND CO·Product code DXY·February 2, 2007

RETROX 45 JBP

FDA Adverse Event
Malfunction ·BIOTRONIK GMBH AND CO.·Product code DTB·February 2, 2007

PHILOS II SR

FDA Adverse Event
Malfunction ·BIOTRONIK GMBH AND CO.·Product code DTB·February 2, 2007

BARCOMED 2MP2

FDA 510(k)
FDA Class 2 ·Radiology

INSTANT-VIEW METHADONE URINE CASSETTE TEST

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

SPECTRA WAVEWRITER

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·November 29, 2024

4.5MM LCP PROXIMAL FEMUR PLATE 10 HOLES/283MM-LEFT

FDA Adverse Event
Injury ·SYNTHES USA·Product code HRS·April 22, 2013

HOMECHOICE AUTOMATED PD SET WITH CASSETTE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·April 26, 2011

GE OEC 9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·July 9, 2008

Coronary Drug-Eluting Stent

FDA Pre-Market Approval
FDA Class 3 ·XIENCE AND PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEMS

LOGIC CR TIB INSERT STD, SZ 3, 9MM

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·April 3, 2024

ZENITH® TX2® TAA ENDOVASCULAR GRAFT PROXIMAL TAPERED COMPONENT

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code MIH·August 8, 2018

MINIMED 780G OUS SYSTEM BLE CONNECT 3.0 MG/DL

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·January 21, 2022

Coronary Drug-Eluting Stent

FDA Pre-Market Approval
FDA Class 3 ·XIENCE V & PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEMS

Coronary Drug-Eluting Stent

FDA Pre-Market Approval
FDA Class 3 ·XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM (EECSS)