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

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NEXUS MIDLINE CT CATHETER

FDA 510(k)
FDA Class 2 ·General Hospital

Cancellous Screw, Cannulated

FDA UDI
I.T.S. GmbH·09120034302299·Cancellous Screw, Cannulated, D=4.0mm, L=70mm, ...

Mariner Outrigger

FDA UDI
Seaspine Orthopedics Corporation·10889981179809·Z-Rod, Dia. 6.0mm, Co-Cr, 270mm

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197052405·Micro-Halstead-Mosquito Hemost. Forceps straig...

ARTISAN AESTHETIC SYSTEM

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

OPUSDUO; OPUSDUO E; OPUSDUO EC; OPUS 20; OPUS SPECTRUM

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

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·October 26, 2021

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·August 17, 2023

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·October 18, 2021

PRECISION

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·April 20, 2020

LONG NAIL KIT R2.0, TI, RIGHT GAMMA3 11X300MM X 1

FDA Adverse Event
Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·June 19, 2012

HOMECHOICE AUTOMATED PD SET WITH CASSETTE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·May 31, 2013

HOMECHOICE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 26, 2011

DEXTRUS 4136

FDA Adverse Event
Injury ·BIOTRONIK GMBH AND CO.·Product code DTB·August 29, 2008

Exactech Equinoxe CAGE GLENOID,POSTERIOR AUGMENT, CEMENTED, Right, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-13-32, b) 41, 44, 47, 50, head, Medium, Item Number 314-13-33, c) 44, 47, 50, 53 head, Large, Item Number 314-13-34, d) 44, 47, 50, 53 head, Extra Large, Item Number 314-13-35; Shoulder Arthroplasty

FDA Enforcement
Class II ·Ongoing·Exactech, Inc.·April 10, 2024